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Search Jobs by Category
| Johnson & Johnson Family of Companies |
Charleston |
WV |
11/19/2009
|
| LAB SPECIALIST (WEST VIRGINIA) |
| A minimum of a Bachelor's degree with concentration in Medical Technology or similar science concentration is required. A minimum of two years of experience as a Medical Technologist or related experience is required. Advanced Technical Certification or experience is also desired. Previous Blood Banking experience is preferred. Experience working with or training individuals on laboratory equipment. A Valid US Driver's License is required. Experience as a Chemistry/Blood Bank Supervisor or Laboratory Manager and/or Specialist is desired. Approximately 75% travel will be required for this position. This position will be based in West Virginia. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Green Bay |
WI |
11/19/2009
|
| Northern, WI : Orthovisc Sales Representative: DePuy Mitek, Inc., Unit of DePuy, Inc. |
| To be considered for this position, candidates must possess a minimum of a 4-year undergraduate college degree and aptitude for field sales. 1-3 year's field sales or field support experience preferable within pharmaceutical, biotech, or medical industries. A valid drivers license issued in one of the 50 States and clean driving record are mandatory. Good written and oral communication skills is required. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Seattle |
WA |
11/19/2009
|
| Seattle, WA: Alternate Care Representative: Ethicon Products, Unit of Ethicon Inc. |
| To be considered for this role, candidates must meet the following criteria: A minimum of a Bachelor's degree, at least three years of outside selling experience, excellent written and oral communication skills, a valid driver's license and clean driving record, the ability to travel as necessary (potentially overnight and/or weekend) is preferred required. The ability to work in a lab or an operating room environment is also required. It is preferred that candidates have documented successful sales performance (high growth, results vs. plan). Be a self-starter with strong time management and planning skills, have the ability to target accounts and achieve results through a daily action plan, and be able to collaborate with other J&J associates (peers, marketing, Strategic Account Managers), external companies (distributors) and KOL's. Suture Sales experience and Distribution Sales is highly preferred but not required. If you want to explore the many small-company environments behind the big company impact of the Johnson & Johnson Family of companies, bid on this position today. |
| Novartis Oncology |
na |
WA |
11/20/2009
|
| Oncol Area Sales Manager/Sr Area Sales Manager |
| Bachelor's degree required with a minimum of three years of pharmaceuticals sales management experience in the oncology, institutional, or specialty marketplace. Qualified candidates must have a demonstrated record of success in their ability to lead and inspire a sales team towards meeting and exceeding objectives, to communicate and implement tactical product strategies with a sophisticated audience, and to think strategically (i.e., "outside the box" and look at the "big picture") while providing creative and innovative solutions to market problems. Personal integrity and leadership abilities are essential. Excellent interpersonal, communication (both written and verbal), and presentation skills are required. Must be able to effectively multitask, problem-solve, and make decisions. Computer literacy (i.e., Word, Excel, and PowerPoint) is a must. As one of the largest pharmaceutical companies in the world and voted as one of the 100 Best Companies to work for by Working Mother Magazine, we are committed to peak performance, improving the quality of life, and embracing and leveraging diverse backgrounds, cultures and talents to achieve competitive advantage. Novartis is an equal opportunity employer M/F/D/V |
| Novartis Oncology |
na |
WA |
11/20/2009
|
| Psychiatry Sales Specialist - Spokane, WA FW2HHE |
| Bachelors degree (preferably in Life Sciences, Pharmacy or Business related discipline).
Minimum two years of pharmaceutical specialty sales experience.
At least one year of pharmaceutical sales experience in the institutional sector, preferably with Psychiatrists.
Familiarity with the Psychiatric community is a plus.
This position may require significant travel due to the large geography that the incumbent will be responsible for.
Must work within 50 miles of the region?s border.
Novartis is committed to embracing and leveraging diverse backgrounds, cultures and talents to achieve competitive ad-vantage. Novartis is an equal opportunity employer M/F/D/V |
| Novartis Oncology |
na |
WA |
11/20/2009
|
| Psychiatry Sales Specialist - Seattle South, WA FW2H1B |
| Bachelors degree (preferably in Life Sciences, Pharmacy or Business related discipline).
Minimum two years of pharmaceutical specialty sales experience.
At least one year of pharmaceutical sales experience in the institutional sector, preferably with Psychiatrists.
Familiarity with the Psychiatric community is a plus.
This position may require significant travel due to the large geography that the incumbent will be responsible for.
Must work within 50 miles of the region?s border.
Novartis is committed to embracing and leveraging diverse backgrounds, cultures and talents to achieve competitive ad-vantage. Novartis is an equal opportunity employer M/F/D/V |
| Novartis Oncology |
na |
WA |
11/20/2009
|
| Psychiatry Sales Specialist - Seattle South, WA FW2H2B |
| Bachelors degree (preferably in Life Sciences, Pharmacy or Business related discipline).
Minimum two years of pharmaceutical specialty sales experience.
At least one year of pharmaceutical sales experience in the institutional sector, preferably with Psychiatrists.
Familiarity with the Psychiatric community is a plus.
This position may require significant travel due to the large geography that the incumbent will be responsible for.
Must work within 50 miles of the region?s border.
Novartis is committed to embracing and leveraging diverse backgrounds, cultures and talents to achieve competitive ad-vantage. Novartis is an equal opportunity employer M/F/D/V |
| Novartis Oncology |
na |
WA |
11/20/2009
|
| Psychiatry Area Sales Manager - Seattle, WA |
| Bachelors degree (preferably in Life Sciences, Pharmacy or Business related discipline). Masters degree/MBA preferred.
Must live within 50 miles of the Area?s border.
Three or more years of pharmaceutical sales experience.
At least two years of pharmaceutical sales management experience.
Preferred Qualifications: Previous experience within the anti-psychotics class or schizophrenia disease state. Calling on psychiatrists and or institutions is a plus.
This position may require significant travel due to the large geography that the incumbent will be responsible for. |
| Novartis Oncology |
na |
WA |
11/20/2009
|
| Hematology Sales Representative/Specialist - Spokane, WA |
| Bachelor?s Degree 5 years of pharmaceutical sales experience At least 2 years of experience in oncology/urology/institutional/specialty sales. Computer literacy i.e., Word, Excel, PowerPoint Candidates must be self-motivated, possess a high degree of technical expertise, have exceptional selling skills, be team-oriented and must be familiar with the Oncology community. Novartis is committed to embracing and leveraging diverse backgrounds, cultures and talents to achieve competitive advantage. Novartis is an equal opportunity employer M/F/D/V. |
| Biogen Idec, Inc. |
Seattle |
WA |
11/20/2009
|
| Senior Program Officer - Agricultural Development |
• Minimum of ten years experience in the development and management of projects involving crop improvement, crop management, extension research and/or seed systems for Africa or South Asia
• A PhD or other advanced degree in a discipline relevant to crop improvement, including plant breeding, molecular marker applications, agronomy or a closely related field
• The capacity to think through, evaluate, justify, and make major investments in agricultural research and development
• An outstanding record of achievement and leadership in the field
• Experience developing, managing, and implementing project strategies and the negotiation, execution, conduct and management of performance-based contracts
• Experience with grants or cooperative agreements
• Ability to think/work at scale as well as “work in white space,” create new ideas, strategize with passionate commitment to a successful outcome
• Demonstrated excellent written and oral communication skills in positions requiring communication with a broad and diverse audience
• Ability to prioritize, focus, and achieve results in a fast paced environment
• Track record of working well with others in teams; sense of humor
• Selfless dedication to the mission, flexibility, and willingness to learn
• Overseas experience and the ability to travel internationally |
| Johnson & Johnson Family of Companies |
Spokane |
WA |
11/19/2009
|
| LAB SPECIALIST- Spokane, Washington Area |
| A minimum of a Bachelor's degree with concentration in Medical Technology or similar science concentration is required. A minimum of two years of experience as a Medical Technologist or related experience is required. Advanced Technical Certification or experience is also desired. Previous Blood Banking experience is strongly preferred. Experience working with or training individuals on laboratory equipment. A Valid US Driver's License is required. Experience as a Chemistry/Blood Bank Supervisor or Laboratory Manager and/or Specialist is desired. Approximately 70% travel will be required for this position. This position will based in Spokane, Washington Area. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Seattle |
WA |
11/19/2009
|
| Washington/Montana: Sales Representative - Cordis Corporation, Cardiology |
| To be considered for this role, candidates must meet the following criteria: BA/BS in a life science or business; and a minimum of 3 years of outside sales experience. Medical device sales experience paired with Cardiology sales experience strongly preferred. Valid drivers license and clean driving record is mandatory. Candidates must be able to travel overnight as needed or requested, and must possess good written and oral communication skills. By choosing Cordis Corporation, you are choosing to positively impact the lives of millions of people each year! |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Sr. Engineer - Sterile Process/Capital Project Support |
| Requirements:Bachelor of Science in Chemical Engineering, Mechanical Engineering, or Biomedical Engineering5 years experience in a process engineering support or capital project engineering role supporting an FDA regulated processPreferred:Experience with a sterile/aseptic processExperience with a pharmaceutical manufacturing process Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. We offer an excellent salary and an industry-ranked benefits program, including tuition reimbursement, work-life balance initiatives and developmental programs at all levels. Merck's retirement package includes a pension plan and one of the best 401(k) plans in the nation. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition #CHE002167. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Our work is someone's hope. Join us.Where patients come first - Merck Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Merck Manufacturing Engineering Intern |
| This position requires applicant to be currently working toward a Bachelors degree in Chemical Engineering, Biochemical Engineering, Biomedical Engineering (process option), Mechanical Engineering, Electrical Engineering or related field. Must be available for 10 week internship beginning June 2010. Candidate must be eligible to work in the U.S. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # ADM003928. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Staff Engineer - Fermentation Process Support |
| Required:Bachelor degree in Engineering or Science field 2 years experience in an engineering or operations position supporting a manufacturing process through one or more of the following roles: process improvements, monitoring process performance, investigating atypicals and implementing corrective actions, creating standard work for operations, and assisting in troubleshooting of the process. Preferred:Experience with technical support of a GMP (good manufacturing practices) manufacturing process BS degree in Chemical Engineering, Biotechnology, Chemistry/Biochemistry Experience in bioprocess manufacturing Experience with fermentation and/or purification processes for production of proteins Supervisory experience Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # CHE002156. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Manufacturing Development Program |
| This position requires candidate to be currently enrolled in a MS program in Chemical Engineering, Biochemical Engineering, BioMedical Engineering (process option), Mechanical Engineering, Industrial Engineering, Chemistry/ Biochemistry, Biology/ Microbiology, or Supply Chain Management. Ideal candidate will possess superior communication and interpersonal skills. Must be graduating between August 2009 and August 2010. Candidates must be eligible to work in the US without sponsorship. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # CHE002049. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Safety and Industrial Hygiene Manager |
| Requirements: Bachelor's degree required. Concentrations in Safety, or Industrial Hygiene strongly preferred. Relevant professional certifications and/or Six Sigma Green belt a plus. Minimum of 10 years applied safety professional work experience in a pharmaceutical, chemical or manufacturing environment, coupled with 3 years in a position of safety program leadership. Excellent leadership, program management, project management, and organizational skills. Demonstrated experience in developing facilities to meet OSHA VPP certification criteria or equivalent. Broad based knowledge of safety regulations. Customer focus-team building, proactive style. Excellent verbal and written communication skills. Proven record interpersonal and negotiation skills. Provenience in MS Word, MS Excel, MS Powerpoint. Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. We offer an excellent salary and an industry-ranked benefits program, including tuition reimbursement, work-life balance initiatives and developmental programs at all levels. Merck's retirement package includes a pension plan and one of the best 401(k) plans in the nation. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # ENV000115.Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Our work is someone's hope. Join us.Where patients come first - Merck Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Environmental Services Manager |
| Requirements: Bachelor's required. Concentrations in an environmental discipline highly preferred. Relevant professional certifications and/or Six Sigma Green Belt a plus. Minimum 10 years applied environmental professional work experience in a pharmaceutical, chemical or manufacturing environmental, coupled with 3 years in a position of environmental program leadership. Proficient in federal and state and regulatory programs. Excellent leadership, program management, project management, and organizational skills. Excellent verbal and written communication skills. Excellent interpersonal and negotiation skills. Proficiency in MS Word, MS Excel, MS Powerpoint. Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. We offer an excellent salary and an industry-ranked benefits program, including tuition reimbursement, work-life balance initiatives and developmental programs at all levels. Merck's retirement package includes a pension plan and one of the best 401(k) plans in the nation. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # ENV000114. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Our work is someone's hope. Join us.Where patients come first - Merck Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Staff Engineer - Sterile Process/Capital Project Support |
| Requirements:Bachelor of Science in Chemical Engineering, Mechanical Engineering, or Biomedical Engineering 2 years experience in a process engineering support or capital project engineering role supporting an FDA regulated process Preferred:Experience with a sterile/aseptic process Experience with a pharmaceutical manufacturing process Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition #CHE002165. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Process Engineer/Scientist - Pharmaceutical Manufacturing Process Support |
| Basic Qualifications: Bachelor's degree in Chemical, BioChemical or Bioprocess Engineering with 7 years experience in a GMP Biopharmaceutical manufacturing or research and development environment OR Master's degree in Chemical, BioChemical or Bioprocess Engineering with 5 years experience in a GMP Biopharmaceutical manufacturing or research and development environment OR PhD in Chemical, BioChemical or Bioprocess Engineering Preferred Qualifications:Experience leading and developing people and teams Experience and expertise in protein purification or fermentation Project management experience Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. We offer an excellent salary and an industry-ranked benefits program, including tuition reimbursement, work-life balance initiatives and developmental programs at all levels. Merck's retirement package includes a pension plan and one of the best 401(k) plans in the nation. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # CHE002084. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Our work is someone's hope. Join us.Where patients come first - Merck Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Sr. Engineer/Scientist - Manufacturing Process Technical Support |
| Minimum Qualifications: Bachelor's degree in Chemical, BioChemical or Bioprocess Engineering with 5 years experience in a GMP Biopharmaceutical manufacturing or research and development environment OR Master's degree in Chemical, BioChemical or Bioprocess Engineering with 2 years experience in a GMP Biopharmaceutical manufacturing or research and development environment Preferred Qualifications:Experience providing technical support of a GMP manufacturing process, specifically in protein purification and/or fermentation. Experience writing technical documentation: such as change controls, protocols, operating procedures. Experience with commissioning, qualification, and validation of biopharmaceutical equipment and processes. Demonstrated expertise in bioprocessing unit operations such as fermentation, chromatography, tangential flow filtration Demonstrated ability to lead a group of individuals in task oriented assignments such as technical investigations, root cause analysis, equipment installation Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. We offer an excellent salary and an industry-ranked benefits program, including tuition reimbursement, work-life balance initiatives and developmental programs at all levels. Merck's retirement package includes a pension plan and one of the best 401(k) plans in the nation. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # CHE002082. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Our work is someone's hope. Join us.Where patients come first - Merck Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Novartis Oncology |
na |
VA |
11/20/2009
|
| Psychiatry Sales Specialist - Roanoke, VA FS2A2A |
| Bachelors degree (preferably in Life Sciences, Pharmacy or Business related discipline).
Minimum two years of pharmaceutical specialty sales experience.
At least one year of pharmaceutical sales experience in the institutional sector, preferably with Psychiatrists.
Familiarity with the Psychiatric community is a plus.
This position may require significant travel due to the large geography that the incumbent will be responsible for.
Must work within 50 miles of the region?s border.
Novartis is committed to embracing and leveraging diverse backgrounds, cultures and talents to achieve competitive ad-vantage. Novartis is an equal opportunity employer M/F/D/V |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Staff Engineer - Protein Purification |
| Required:Bachelors degree in Engineering or Science Discipline 2 years experience in a GMP regulated environment with some or all of that time spent in an Engineering role in support of a process that includes protein purification (will consider a Master's degree in Chemical Engineering, BioChemical Engineering or Biomedical Engineering in lieu of experience) Preferred:Experience with a facility start up Experience with validation qualifications for a start up facility Engineering support experience with a vaccine product Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition #CHE002144. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Manufacturing Technical Rotation |
| This position requires candidate to be currently enrolled in a MS program in Chemical Engineering, Biochemical Engineering, BioMedical Engineering (process option), Bioengineering, or related field. Ideal candidate will possess superior communication and interpersonal skills. Must be graduating between August 2009 and August 2010. Candidates must be eligible to work in the US without sponsorship. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # CHE002052. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Manufacturing Technical Rotation |
| This position requires candidate to be currently enrolled in a PhD program in Chemical Engineering, Biochemical Engineering, BioMedical Engineering (process option), Bioengineering, or related field. Ideal candidate will possess superior communication and interpersonal skills. Must be graduating between August 2009 and August 2010. Candidates must be eligible to work in the US without sponsorship. Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # CHE002053. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Merck Manufacturing Engineering Intern |
| This position requires applicant to be currently working toward a Bachelors degree in Chemical Engineering, Biochemical Engineering, Biomedical Engineering (process option), Mechanical Engineering, Electrical Engineering or related field. Must be available for 10 week internship beginning June 2010. Candidate must be eligible to work in the U.S. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # ADM003868. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Merck Manufacturing Science Intern |
| This position requires applicant to be currently working toward a Bachelors degree in Biology, Microbiology, Virology, Chemistry or Biochemistry. Must be available for 10 week internship beginning June 2010. Candidate must be eligible to work in the U.S. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition #ADM003932 Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Merck Manufacturing Engineering Intern |
| This position requires applicant to be currently working toward a Bachelors degree in Chemical Engineering, Biochemical Engineering, Biomedical Engineering (process option), Mechanical Engineering, Electrical Engineering or related field. Must be available for 10 week internship beginning June 2010. Candidate must be eligible to work in the U.S. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # ADM003908. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Merck Manufacturing Engineering Intern |
| This position requires applicant to be currently working toward a Bachelors degree in Chemical Engineering, Biochemical Engineering, Biomedical Engineering (process option), Mechanical Engineering, Electrical Engineering or related field. Must be available for 10 week internship beginning June 2010. Candidate must be eligible to work in the U.S. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # ADM003898. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Merck Manufacturing Graduate Intern |
| This position requires applicant to be currently working toward a working toward graduate degree in Chemical Engineering, Biochemical Engineering, BioMedical Engineering (process option), Statistics or related field. Must be available for 10 week internship beginning June 2010. Candidate must be eligible to work in the U.S. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # MAN000318. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Process Scientist (Adjuvants) |
| The desired candidates will posses a M.S. or PhD in Chemical Engineering or Chemistry (physical and/or analytical) with 1 to 5 years experience (graduate work may count toward this experience). Proven industrial experience with modeling and characterization of aluminum-containing adjuvants in highly desired. To succeed in this role, the candidate will be highly qualified and have a clear understanding of how physical, chemical and engineering properties of processes relate to controlled formation of precipitated particles and to their structure and properties. The candidate should also be familiar with analytical techniques such as X-ray diffraction, FTIR, and/or NMR. Experience with aluminum-containing adjuvant characterization and identification techniques is considered a plus. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition #BIO002469. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| openQ |
Charlottesville |
VA |
11/19/2009
|
| Data Research Project Manager |
| Skills:
• Very thorough understanding of life sciences industry
• Understanding of, and comfort with, reading medical literature and performing information searches on medically-related topics
• Excellent verbal and written communication skills
• Strong analytical skills and technical understanding of data acquisition, data structuring and data quality control
• Prior experience interfacing with customers about data-related projects
• Strong team player and the proven ability to work independently
Education:
• PhD in life sciences field preferred or Master’s degree and preferably at least 5 years relevant experience in life sciences driven data company
|
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Senior Chemist |
| This position requires candidate to be currently enrolled in a PhD program in Chemistry or Biochemistry. Ideal candidate will possess superior communication and interpersonal skills. Must be graduating between August 2009 and August 2010. Candidates must be eligible to work in the US without sponsorship. Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # CHE002034. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Staff Chemical Engineer |
| This position requires candidate to be currently enrolled in a MS program in Chemical Engineering, Biochemical Engineering, BioMedical Engineering (process option), Bioengineering, or related field. Ideal candidate will possess superior communication and interpersonal skills. Must be graduating between August 2009 and August 2010. Candidates must be eligible to work in the US without sponsorship. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # CHE002019. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Merck Manufacturing Development Program |
| This position requires candidate to be currently enrolled in a BS program in Chemical Engineering, Biochemical Engineering, BioMedical Engineering (process option), Mechanical Engineering, Industrial Engineering, Chemistry/ Biochemistry, Biology/ Microbiology, or Supply Chain Management. Ideal candidate will possess superior communication and interpersonal skills, a team player with the ability to work independently. Must be graduating between August 2009 and August 2010. Must be willing to be assigned to different jobs and potentially different sites over the first two years of employment. Candidates must be eligible to work in the US without sponsorship. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # CHE002036. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| sanofi pasteur |
Charlottesville |
VA |
11/19/2009
|
| Vaccine Sales Representative - Charlottesville, VA |
| BA./B.S. in Immunology, Biology, Business or related field required.
2 years business to business sales or equivalent experience.
Strong oral, written and analytical skills with the demonstrated ability to work in teams.
Strong time management skills
Certifications
Driver's license is required along with a record of safe driving |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Biologist |
| This position requires candidate to be currently enrolled in a BS level program in Biology, Microbiology, Virology. Successful candidates will possess superior communication and interpersonal skills. Laboratory experience is preferred. Must be graduating between August 2009 and August 2010. Candidates must be eligible to work in the US without sponsorship. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # BIO002391. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| sanofi pasteur |
Blacksburg |
VA |
11/19/2009
|
| Vaccine Sales Representative - Blacksburg, VA |
| BA./B.S. in Immunology, Biology, Business or related field required.
2 years business to business sales or equivalent experience.
Strong oral, written and analytical skills with the demonstrated ability to work in teams.
Strong time management skills
Certifications
Driver's license is required along with a record of safe driving |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Sr. Engineer - Protein Purification |
| Required:Bachelors degree in Engineering or Science Discipline 5 years experience in a GMP regulated environment with some or all of that time spent in an Engineering role in support of a process that includes protein purification Preferred:Experience with a facility start up Experience with validation qualifications for a start up facility Engineering support experience with a vaccine product Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition #CHE002143. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Biologist |
| This position requires candidate to be currently enrolled in a BS level program in Biology, Microbiology, Virology. Successful candidates will possess superior communication and interpersonal skills. Laboratory experience is preferred. Must be graduating between August 2009 and August 2010. Candidates must be eligible to work in the US without sponsorship. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # BIO002401. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Chemical Engineer |
| This position requires candidate to be currently enrolled in a BS program in Chemical Engineering, Biochemical Engineering, BioMedical Engineering (process option), Bioengineering, or related field. Ideal candidate will possess superior communication and interpersonal skills. Must be graduating between August 2009 and August 2010. Candidates must be eligible to work in the US without sponsorship. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # CHE001978. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| BD (Becton, Dickinson and Company) |
Sandy |
UT |
11/20/2009
|
| Mechanical Engineer w/ FEA, Medical Surgical Systems |
| See above |
| BD (Becton, Dickinson and Company) |
Sandy |
UT |
11/20/2009
|
| Product Manager |
| See above |
| BD (Becton, Dickinson and Company) |
Sandy |
UT |
11/20/2009
|
| Process Technician/Mold Set Up -- Trainee |
| See above |
| BD (Becton, Dickinson and Company) |
Sandy |
UT |
11/20/2009
|
| Process Technician |
| See above |
| BD (Becton, Dickinson and Company) |
Sandy |
UT |
11/20/2009
|
| Mechanical Design Engineer, Medical Surgical Systems |
| See above |
| BD (Becton, Dickinson and Company) |
Sandy |
UT |
11/20/2009
|
| Engineering Technician |
| See above |
| Novartis Oncology |
na |
UT |
11/20/2009
|
| Psychiatry Sales Specialist - Salt Lake City, UT FW2F2E |
| Bachelors degree (preferably in Life Sciences, Pharmacy or Business related discipline).
Minimum two years of pharmaceutical specialty sales experience.
At least one year of pharmaceutical sales experience in the institutional sector, preferably with Psychiatrists.
Familiarity with the Psychiatric community is a plus.
This position may require significant travel due to the large geography that the incumbent will be responsible for.
Must work within 50 miles of the region?s border.
Novartis is committed to embracing and leveraging diverse backgrounds, cultures and talents to achieve competitive ad-vantage. Novartis is an equal opportunity employer M/F/D/V |
| BD (Becton, Dickinson and Company) |
Sandy |
UT |
11/20/2009
|
| Sr. Electro-Mechanic |
| See above |
| BD (Becton, Dickinson and Company) |
Sandy |
UT |
11/20/2009
|
| Principal Scientist, Advanced Technology - Medical Surgical Systems |
| See above |
| BD (Becton, Dickinson and Company) |
Sandy |
UT |
11/20/2009
|
| VP Manufacturing Infusion |
| See above |
| BD (Becton, Dickinson and Company) |
Sandy |
UT |
11/20/2009
|
| Quality Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Sandy |
UT |
11/20/2009
|
| R&D Manager, Infusion Systems |
| See above |
| BD (Becton, Dickinson and Company) |
Sandy |
UT |
11/20/2009
|
| Regulatory Compliance Complaint Analyst |
| See above |
| Novartis Oncology |
na |
UT |
11/20/2009
|
| Regl Account Scientific Asc Dir/Director (AZ, CO, NM, NV and UT) |
| Position will be filled at level commensurate with experience.
MD, PharmD, or PhD with 4 years Post-Doctoral experience required. Field-based medical and/or managed care experience preferred. Thorough knowledge of clinical medicine, managed markets, pharmacoeconomics, disease management, and medical research. Excellent interpersonal communication and presentation skills, (including ability to network), strong personal integrity, teamwork abilities and a customer focus are necessary. Must possess a thorough understanding of the FDA, OIG, HIPAA, and GCP/ICH guidelines relevant to the pharmaceutical industry. Must be able to organize, prioritize, and work effectively in a constantly changing environment. Active membership in professional society(ies) is a plus. Working knowledge of Microsoft Office Suite (Word, PowerPoint, and Excel) and associated hardware is required. Ability to interface effectively with a variety of technical platforms for the collection, review, and dissemination of medical information. Demonstrated record of scientific/medical publication. Demonstrated knowledge of GCP practices and standards. Demonstrated technical expertise in at least one disease or therapeutic area. The RASM/D position is associated with approximately 60% travel. Salary flexible. |
| Johnson & Johnson Family of Companies |
Salt Lake City |
UT |
11/19/2009
|
| Salt Lake City, UT: Full Line Sales Representative: Ethicon Endo-Surgery, Inc. |
| To be considered for this role, candidates must meet the following criteria: A minimum of a Bachelors Degree paired with three or more years of sales experience selling to a highly educated/high profile customer base, or internal EES experience with a proven track record of achieving sales & competency objectives as an Associate Sales Representative. The ability to sell in an operating room, lab & hospital environment is required. A valid driver's license issued in one of the 50 States with a clean driving record is required. The ability to travel as necessary, which may include overnight and/or weekends, is required. Medical device sales experience is preferred paired with documented sales results. Individuals must live within the current geography or be willing to relocate to it. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Salt Lake City |
UT |
11/19/2009
|
| Salt Lake City, UT: Sales Representative - Cordis Corporation, Cardiology |
| To be considered for this role, candidates must meet the following criteria: BA/BS in a life science or business; and a minimum of 3 years of outside sales experience. Medical device sales experience paired with Cardiology sales experience strongly preferred. Valid drivers license and clean driving record is mandatory. Candidates must be able to travel overnight as needed or requested, and must possess good written and oral communication skills. By choosing Cordis Corporation, you are choosing to positively impact the lives of millions of people each year! |
| Johnson & Johnson Family of Companies |
San Antonio |
TX |
11/19/2009
|
| San Antonio, Texas - Territory Assistant: Ethicon Products, Unit of Ethicon, Inc. |
| Qualified candidates will have a minimum of a Bachelors Degree coupled with at least 2 years of solid Business to Business sales with demonstrated results. Candidates should have experience in product sales to a highly educated/high profile customer base. Candidates with Medical Device, Surgical or Capital equipment experience are preferred. Must be willing to work in an Operating Room environment. Candidates must have a valid driver's license and clean driving record (no more than 2 moving violations and/or accidents within a 6 month period and no more that 3 in a 3 year period). A current method of effectively targeting accounts and achieving results through a daily action plan. Important: This job requires the candidate to be willing to relocate and/or travel at any given time based on the needs of the company within the geographical sales region. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
San Antonio |
TX |
11/19/2009
|
| San Antonio, TX: Associate Sales Representative: Ethicon Endo-Surgery, Inc. |
| To be considered for this role, a Bachelor's degree is required. The ability to travel as necessary, depending on geography (potentially overnight and/or weekends) and willingness to relocate nationally within the first year of employment is required. Two years of outside selling experience is preferred. Candidates must have a valid driver's license in one of the 50 states and clean driving record, as well as excellent written and oral communication skills. Candidate's must either be in active military service or within 12 months of active service or within 12 months of receiving their college degree. Candidates with documented successful sales performance (high growth, results vs. plan), the ability to target accounts and achieve results through a daily action plan and the ability to collaborate with other J&J associates (peers, marketing, Strategic Account Managers), external companies (distributor reps) and KOLs, is preferred. Self-starters with strong time management and planning skills are also a plus. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Houston |
TX |
11/19/2009
|
| Houston, TX: Territory Business Manager - Vistakon, Johnson & Johnson Vision Care, Inc. |
| To be considered for this role, the candidate must have at least a Bachelor's Degree, coupled with at least 3 years of business-to-business and/or medical sales experience. Candidates must have a valid driver's license issued in one of the 50 States and a clean driving record. The ability to travel as necessary, which may include overnight and/or weekend travel is required. Candidates must also have excellent written and oral communication skills. Preference will be given to candidates with documented sales awards and achievements, prior management development training and/or have taken career development classes or completion of a major sales training course. Preference will also be given to candidates living within 30 miles of the posted territory. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson, Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Houston |
TX |
11/19/2009
|
| Houston, TX: Alternate Care Representative: Ethicon Products, Unit of Ethicon Inc. |
| To be considered for this role, candidates must meet the following criteria: A minimum of a Bachelor's degree, at least three years of outside selling experience, excellent written and oral communication skills, a valid driver's license and clean driving record, the ability to travel as necessary (potentially overnight and/or weekend) is preferred required. The ability to work in a lab or an operating room environment is also required. It is preferred that candidates have documented successful sales performance (high growth, results vs. plan). Be a self-starter with strong time management and planning skills, have the ability to target accounts and achieve results through a daily action plan, and be able to collaborate with other J&J associates (peers, marketing, Strategic Account Managers), external companies (distributors) and KOL's. Suture Sales experience and Distribution Sales is highly preferred but not required. If you want to explore the many small-company environments behind the big company impact of the Johnson & Johnson Family of companies, bid on this position today. |
| Johnson & Johnson Family of Companies |
Irving |
TX |
11/19/2009
|
| Lean Manufacturing Engineer |
| A minimum of a Bachelor's degree in Mechanical, Industrial, Electrical or Chemical Engineering required. A Master's degree preferred. A minimum of 3 years experience of process improvement experience required. Black Belt Certification required. PMP Certification preferred. Advanced computer skills and use of software applications such as iGrafx or similar software is required. Must have excellent analytical and statistical skills. Knowledge of Lean Manufacturing principles, including: Value Stream Mapping, Kaizen, One-Piece Flow, Kanban, Cellular Manufacturing, Six Sigma, Set-up Reduction, Visual Management, required. Must have proven initiative, creativity, assertiveness and leadership abilities. Must be able to work under pressure, achieving consistently high results through individual and team efforts. Must have excellent interpersonal, influencing, communication, presentation, listening, negotiating and problem-solving/decision-making skills. Must have the ability to set priorities and achieve objectives. Project management and cost/benefit analysis experience required. Capacity Planning experience, including productivity measurements, manpower planning and material flow, is required. Must have the ability to read, analyze and interpret common scientific, technical journals and financial reports. Must have the ability to write reports with technical emphasis. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Dallas |
TX |
11/19/2009
|
| Houston/Dallas TX: Clinical Sales Associate: J&J Wound Management: Biosurgicals, Unit of Ethicon, Inc |
| To be considered for this role, candidates must meet the following criteria: A minimum of a Bachelor's degree. A minimum one year of outside sales experience is required. Medical Device sales experience strongly preferred. 2-5 years combined medical device and competitive business-to-business sales experience preferred. A valid driver's license issued in one of the fifty states and a clean driving record is required. The ability to work in a hospital/operating room environment is required. Willingness to travel up to 40% depending on geography is required. To be eligible for this position, applicants must currently reside in the posted territory or be willing to relocate there at their own expense. Willingness to relocate within 12 - 18 months of employment is required. If you want to explore the many small-company environments behind the big company impact of the Johnson & Johnson Family of companies, bid on this position today! |
| Agilent Technologies, Inc. US |
Cedar Creek |
TX |
11/20/2009
|
| Manufacturing Associate-Intermediate |
| This position requires a BS/BA degree in biological science or related field and one (1) to two (2) years of previous experience in chemistry, molecular biology and/or biochemistry. A strong working knowledge of standard laboratory techniques of molecular biology is required ( PCR, DNA and RNA isolation, bacterial transformations). Strong oral and written communication, organization, team building and computer skills essential.
cb~11/11/2009 |
| Agilent Technologies, Inc. US |
Houston |
TX |
11/20/2009
|
| Service Sales Specialist ? Southern US Region |
| Requires
- BS/MS in Scientific, Engineering or Business discipline or equivalent.
- 3+ years hands on laboratory or industry experience with instrumentation hardware, software, applications coupled with industry regulatory requirements such as (GLP, GMP, FDA) highly desired
- 3+ years sales experience with a demonstrated track record of success in projects or sales at major accounts highly desired.
- Ability to translate the Value Proposition of service as a financial and operational benefit to meet customer needs.
- Strong business development, sales negotiating, and sales closing skills.
- Must have excellent communication skills (written and verbal) and teamwork skills.
- Outstanding presentation, planning and organizational skills
- High level knowledge of instrument support services business
- Computer literate with advanced skills using Microsoft suite of products (Outlook, Excel, Word, Powerpoint, Access) plus other IT systems.
- Able to interface comfortably at high levels within the customer management structure
- Demonstrated attention to detail and ability to manage large volumes of data.
- Must be available for up to 60% business travel
- Live in Houston, or surrounding communities
Region Includes: Texas, Oklahoma, Louisiana
~cb~11/09/09 |
| Agilent Technologies, Inc. US |
Richardson |
TX |
11/20/2009
|
| Application Engineer |
| Education:
B.S.E.E and/or M.S.E.E. preferred
Experience:
-5+ years of practical RF design engineering experience.
-2 years of which will be relevant industry experience.
-Ability to fully understand customer needs and the technical ability to fulfill them.
-Understanding of RAT's (Radio Access Technology), in 2G/3G systems like GSM, WCDMA, HSPA. WiMax, LTE and MIMO experience a plus.
-Understanding applied use of advanced one box testers, signal generators and spectrum analyzers.
Geo Location: Richardson, Texas
~cb~11/05/09 |
| Agilent Technologies, Inc. US |
Cedar Creek |
TX |
11/20/2009
|
| Distribution Associate I |
| ? High school diploma or general education degree (GED); or zero (0) to three (3) years related experiences and/training; or equivalent combination of education and experience.
? Ability to demonstrate an understanding at a level that may include addition, subtraction, multiplication and division in all units of measure using whole numbers, common fractions and decimals.
? Ability to read and interpret at a level that may include documents such as safety rules, operating instructions and procedural manuals.
? Ability to apply common sense understanding to carry out instructions furnished in written, oral or diagram form. Requires basic computer operations skills. Awareness and or ability to use Microsoft Office Suite tools.
Certification:
? Forklift Operator Certification, required within 90 days.
Other skills:
? Knowledge of commonly used practices and procedures within distribution and warehousing.
Physical demands:
? The physical demands described here are representative of those demands that must be met by the employee to successfully perform the essential functions of the job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
? While performing the duties of this job, the employee is regularly required to stand, walk, reach with hand and arms, sit, climb, balance or stoop, kneel, crouch or crawl, regularly lift and/or move up to 15 pounds and occasionally lift and/or move up to 100 pounds. Specific vision abilities required include accurate close vision, distance vision and depth perception.
Work Environment:
? The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of the job. While performing the duties of this job, the employee is frequently exposed to extreme cold and loud noises. the employee is occasionally exposed to moving mechanical parts, high, precarious places and toxic or caustic chemicals requiring steel toed shoes to be worn at all times and occasionally hard hats. |
| Johnson & Johnson Family of Companies |
Lubbock |
TX |
11/19/2009
|
| Lubbock, TX - Territory Manager - Animas |
| To be considered for this role, candidates must meet the following criteria: Minimum of a Bachelor's Degree. 3+ years of healthcare related sales experience is required. 2+ years medical device sales experience is preferred. Candidates must have a valid driver's license issued in one of the 50 United States and a clean driving record. Ability to demonstrate having consistently exceeded objectives in prior positions is required. The ability to travel related to this role is required. An intimate, passionate knowledge of diabetes is preferred. Solid computer skills are required. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Millennium Pharmaceuticals |
Dallas |
TX |
11/19/2009
|
| Health Systems Manager - Dallas |
|
| Novartis Oncology |
na |
TX |
11/20/2009
|
| Psychiatry Sales Specialist - El Paso, TX FW2BHF |
| Bachelors degree (preferably in Life Sciences, Pharmacy or Business related discipline).
Minimum two years of pharmaceutical specialty sales experience.
At least one year of pharmaceutical sales experience in the institutional sector, preferably with Psychiatrists.
Familiarity with the Psychiatric community is a plus.
This position may require significant travel due to the large geography that the incumbent will be responsible for.
Must work within 50 miles of the region?s border.
Novartis is committed to embracing and leveraging diverse backgrounds, cultures and talents to achieve competitive ad-vantage. Novartis is an equal opportunity employer M/F/D/V |
| Johnson & Johnson Family of Companies |
San Angelo |
TX |
11/19/2009
|
| Plant Operations College Hire, Ethicon, Inc. (San Angelo, TX) |
| In order to be eligible for a Fall Co-op position, candidate must be enrolled in an accredited college/institution and be in good academic standing pursuing a Bachelors degree in Industrial Engineering, Electrical Engineering, Mechanical Engineering, Chemical Engineering or related field. Only students in their sophomore year or above will be considered. A minimum GPA of 3.0 is strongly preferred, with demonstrated leadership/participation in campus programs and/or community service activities. Students must be available to work during session indicated and must be authorized to work in the United States and not require sponsorship in the future. |
| Biogen Idec, Inc. |
Houston |
TX |
11/20/2009
|
| Area Business Manager, Neurology - Houston TX |
| Minimum 5+ years pharmaceutical sales or biotech sales experience required. Experience with reimbursement issues, product launch, and injectable/infusion product selling experience desired. |
| Johnson & Johnson Family of Companies |
San Angelo |
TX |
11/19/2009
|
| Controls/Computer Integrated Manufacturing Engineer |
| A minimum of a Bachelors degree in a Computer Science/Engineering, Electrical Engineering, or Computer Integrated Manufacturing discipline with at least two years of programming or design experience is required. Required skills include demonstrated ability to contribute in a team environment supporting 24x7 production operations and continuous improvement programs from a technical improvement standpoint. The ability to supervise personnel would be an asset. In addition, the ability to manage and report project budgets and schedules is a must. Fluency with process/operating specifications and engineering processes and practices is required. Fluency with GMPs, regulations, project management tools (MS Project) would be desired. Knowledge of spreadsheets, word processing and associated software is required. Knowledge of MS Access would be preferred. The candidate should posses a strong work ethic, be self-motivated and able to work with little supervision. Technical competences should include: Object oriented programming is required preferably in .Net framework (VB and/or C#) or VB6 Development environment. Visual Studio 2005/2008 would be preferred, Database experience in Oracle or MS SQL Server highly desired. HMI/ operator interface development - FIX32, IFIX, or RSView preferred. Web programming - ASP/ASP.net, HTML preferred. Basic knowledge with Windows 2000, XP, and/or Vista required. This position will be based in San Angelo, TX. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Dallas |
TX |
11/19/2009
|
| Lab Specialist (Western Texas) |
| A minimum of a Bachelor's degree with concentration in Medical Technology or similar science concentration is required. A minimum of two years of experience as a Medical Technologist or related experience is required. Advanced Technical Certification or experience is also desired. Previous Blood Banking experience is preferred. Experience working with or training individuals on laboratory equipment. A Valid US Driver's License is required. Experience as a Chemistry/Blood Bank Supervisor or Laboratory Manager and/or Specialist is desired. Approximately 75% travel will be required for this position. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Austin |
TX |
11/19/2009
|
| Austin, TX: Territory Manager - Animas Corporation |
| To be considered for this role, candidates must meet the following criteria: Minimum of a Bachelor's Degree. 4+ years of healthcare related sales experience and 2+ years medical device sales experience is preferred. Candidates must have a valid driver's license issued in one of the 50 United States and a clean driving record. Ability to demonstrate having consistently exceeded objectives in prior positions is required. The ability to travel related to this role is required. An intimate, passionate knowledge of diabetes is preferred. Solid computer skills are required. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Radiometer America, Inc. |
Dallas or Houston |
TX |
11/19/2009
|
| Transcutaneous Sales Specialist |
| •Bachelor’s degree in Science (i.e. Biology, Chemistry) or Nursing
•3+ years clinical experience in Respiratory Care, Hyperbaric/Wound Care Medicine or Cardiology
•3+ years medical capital sales experience
•Strong organizational, time management, territory planning skills
•Dynamic, high-energy individual to implement sales activities
•50% travel
If you are unable to apply electronically because of a disability, dial 711 to apply through the Ohio Relay and ask to be connected to the Human Resources Department at 440-871-8900.
Radiometer America Inc. is an equal opportunity / affirmative action employer and does not discriminate on the basis of race, color, gender, national origin, ancestry, religion, martial status, age, veteran status or disability or any other legally protected characteristics that may vary by state, city and/or county of employment.
|
| Johnson & Johnson Family of Companies |
Irving |
TX |
11/19/2009
|
| Maintenance Mechanic (1 of 2) |
| A minimum of a High School diploma is required. Trade school degree preferred. A minimum of 5 years of HVAC, Plumbing and/or Electrical experience is required. Experience as a Maintenance Mechanic in a commercial environment (i.e. manufacturing, industrial) is required. Prior experience in a GMP (Good Manufacturing Practice) or other regulated environment is preferred. Universal EPA certification for refrigerant recovery is required. Experience with CMMS (Computer Maintenance Management Systems) is required. Experience with MP2 is preferred. Basic electrical skills required. Basic computer knowledge is required. Must have excellent communication and practical problem-solving skills. Must have the ability to follow SOPs (Standard Operating Procedures). Knowledge of local and national building codes preferred. The ability to lift and/or move up to 50 pounds is required. Must be a team player and be able to work with minimal technical supervision. Must be able to work a staggered day shift (7:00 a.m. - 3:30 p.m., 11:00 a.m. - 7:30 p.m.), with weekend work and some overtime, requiring rotating on-call duties for any emergencies or alarms during off hours. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Irving |
TX |
11/19/2009
|
| Senior Polymer Engineer |
| A minimum of a Master's or advanced degree in a scientific, engineering, or related discipline is required, with a PhD preferred. A minimum of 5+ years of experience in polymer chemistry or a related discipline is required. Knowledge of product design in relation to Medical Device Directives, ISO13485 and 21CFR820 regulations and standards is required, with knowledge of QSR, Canadian Medical Device Regulations, and Japanese Medical Device Regulations an asset. Hands-on experimentalist background with experience in polymer characterization and silicone chemistry is an asset. Understanding of material characterization, structure-property, and utilization towards intended application is an asset. Experience in medical device product development is required. Experience in medical device process development and regulatory process is an asset. Knowledge of Design/Process Excellence (Six Sigma, Lean, etc.) is an asset. Knowledge of Biostatistics, FEA, and Solidworks is an asset. A demonstrated ability to work independently and in team-oriented environments, embracing change, risk, and flexibility will be needed. Must be capable of handling multiple projects/tasks at the same time as well as the ability to listen to customers' needs and develop solutions to meet their requirements. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Novartis Oncology |
na |
TX |
11/20/2009
|
| Psychiatry Area Sales Manager - Denver, CO |
| Bachelors degree (preferably in Life Sciences, Pharmacy or Business related discipline). Masters degree/MBA preferred.
Must live within 50 miles of the Area?s border.
Three or more years of pharmaceutical sales experience.
At least two years of pharmaceutical sales management experience.
Preferred Qualifications: Previous experience within the anti-psychotics class or schizophrenia disease state. Calling on psychiatrists and or institutions is a plus.
This position may require significant travel due to the large geography that the incumbent will be responsible for. |
| Johnson & Johnson Family of Companies |
Memphis |
TN |
11/19/2009
|
| Maintenance Technician III |
| A minimum of a High School diploma, GED or equivalent degree required. Associate's degree in a technical discipline preferred. Technical school courses and/or previous factory training in Conveyer Systems or building mechanical/electrical/HVAC systems maintenance preferred. A minimum of 5 years of Conveyor Systems maintenance experience required. Experience in the following areas preferred: Programmable Logic Controllers (PLCs), rolling stock (forklift), building mechanical/electrical/HVAC systems. Prior experience in a FDA regulated industry preferred. Packaging machine maintenance experience preferred. Knowledge of maintenance programs and documentation preferred. The ability to work with tools (i.e. hand tools, power tools, etc.) is required. Experience operating a forklift and willingness to become certified as a Forklift Operator required. Must have the ability to follow policies, Standard Operating Procedures (SOPs) and complete work tasks accurately and efficiently. Must have excellent verbal communication skills and demonstrated collaboration skills with team members and management. The ability to lift at least 50 pounds on a repetitive basis, stand and/or walk on concrete floors 90% of the time and bend, twist and perform repetitive tasks are required. The ability to work from heights (i.e. ladders, platforms, and lifts) and under low clearance equipment required. Must be able to work 3rd shift and be available to work other shifts (1st or 2nd). The ability to work overtime, weekends and holidays as needed by business is required. Must be available for rotating on-call duties. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Millennium Pharmaceuticals |
Nashville |
TN |
11/19/2009
|
| Oncology Sales Specialist - Charlotte, NC |
|
| Johnson & Johnson Family of Companies |
Memphis |
TN |
11/19/2009
|
| Memphis, TN: Professional Sales Specialist, Lifescan Inc. |
| A minimum of a 4 year degree is required. Two years of outside sales experience is preferred. 3 years of sales experience in a healthcare professional sales environment or experience in professional diabetes care or related healthcare fields strongly is preferred. Candidates must have a valid driver's license issued in one of the 50 United States and a clean driving record. This position may require overnight and/or weekend travel. Excellent written and oral communication skills are essential. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Novartis Oncology |
na |
TN |
11/20/2009
|
| Psychiatry Area Sales Manager - Nashville, TN |
| Bachelors degree (preferably in Life Sciences, Pharmacy or Business related discipline). Masters degree/MBA preferred.
Must live within 50 miles of the Area?s border.
Three or more years of pharmaceutical sales experience.
At least two years of pharmaceutical sales management experience.
Preferred Qualifications: Previous experience within the anti-psychotics class or schizophrenia disease state. Calling on psychiatrists and or institutions is a plus.
This position may require significant travel due to the large geography that the incumbent will be responsible for. |
| Johnson & Johnson Family of Companies |
Memphis |
TN |
11/19/2009
|
| Senior Logistics Analyst (1 of 2) |
| A minimum of a Bachelor's degree required, preferably in Logistics, Business, Operations, Engineering or related field. MBA preferred. A minimum of 4 years experience in Global Logistics, Supply Chain, Manufacturing or Distribution is required. Experience working in a Good Manufacturing Practices (GMP) environment is preferred. Previous experience in Medical Devices and Diagnostics is preferred. Experience or training in Process Excellence (Lean/Six-Sigma) is required. Process Excellence/Six Sigma certification preferred. Must have excellent verbal and written communication skills. Must have strong organizational and analytical skills. Knowledge of Warehouse Management Systems (i.e. MARC, SAP) preferred. Knowledge of Microsoft Office (Word, Excel, PowerPoint, Outlook) is required. Project management experience preferred. Change leadership experience preferred. Experience collaborating with all levels of management in a cross-functional team environment is required. 5% travel is required. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Memphis |
TN |
11/19/2009
|
| Supervisor, Operations - 3rd Shift |
| A minimum of a High School diploma is required. Bachelor's degree preferred. A minimum of 3 years of experience in Logistics, Operations or a related field is required. A minimum of 2 years of experience managing people, including conducting and delivering performance appraisals is also required. Experience in inventory management, including managing cycle counts, maintaining inventory records and performing inventory adjustments are preferred. Experience using Warehouse Management Systems (i.e. MARC Global) is preferred. Knowledge of Microsoft Office (Word, Excel, PowerPoint, Outlook) is required. Experience with Ariba Procurement System is preferred. Experience with Materials Resource Planning (MRP) Systems is preferred. Experience applying Six Sigma/Process Excellence Tools, Training and/or Certification preferred. Experience working in an Automated Distribution Center environment is preferred. An APICS certification is preferred. Knowledge of Service Level Agreement (SLA) requirements is preferred. Prior experience working in a real-time/fast-paced environment required. Must have strong leadership, interpersonal, analytical and organizational skills. Must have excellent collaboration, customer service and oral/written communication skills. Experience partnering with all levels of management in a cross-functional team environment is required. Must be able to work 3rd shift (11:00 pm - 7:30 am). The ability to work in a refrigerated environment at 2 to 8 C (35 to 46 F) for 2 hours or more at a time and in a freezer at -30 to -20 C (-4 to -22 F) for up to 1 hour at a time is required. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Memphis |
TN |
11/19/2009
|
| Memphis, TN: Sales Representative: Women's Health & Urology, Unit of ETHICON, Inc. |
| A minimum of a Bachelor's degree is required. A miniumm of two years of outside selling experience, excellent written and oral communication skills are also required. A valid driver's license issued in one of the 50 States and clean driving record is required. The ability to travel as necessary (potentially overnight and/or weekend) is required. The ability to work in a lab or an operating room environment is also required. It is preferred that candidates have documented successful sales performance (high growth, results vs. plan). Be a self-starter with strong time management and planning skills, have the ability to target accounts and achieve results through a daily action plan, and be able to collaborate with other J&J associates (peers, marketing, Strategic Account Managers), external companies (distributors) and KOL's. Operating room medical device sales experience is preferred, but not required. If you want to explore the many small-company environments behind the big company impact of the Johnson & Johnson Family of companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Memphis |
TN |
11/19/2009
|
| LAB SPECIALIST, MEMPHIS, TN AREA |
| A minimum of a Bachelor's degree with concentration in Medical Technology or similar science concentration is required. A minimum of two years of experience as a Medical Technologist or related experience is required. Advanced Technical Certification or experience is also desired. Previous Blood Banking experience is preferred. Experience working with or training individuals on laboratory equipment. A Valid US Driver's License is required. Experience as a Chemistry/Blood Bank Supervisor or Laboratory Manager and/or Specialist is desired. Approximately 75% travel will be required for this position. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Novartis Oncology |
na |
SD |
11/20/2009
|
| Territory Sales Manager - Sioux Falls, SD |
| Minimum Education Required:
? Bachelor's degree or equivalent
Minimum Experience Required:
? 2-4 years successful outside sales experience
Preferred Level:
? One (1) year contact lens sales/opthalmic related sales/contact fitting experience.
Must have valid drivers license and the ability to travel extensively via automobile. Some air travel also required. Must successfully complete our ""New Hire Sales Training Program"". |
| Johnson & Johnson Family of Companies |
Columbia |
SC |
11/19/2009
|
| Columbia, SC: Breast Care Specialist: Ethicon Endo-Surgery, Inc. |
| To be considered for this role, candidates must meet the following criteria: A minimum of a Bachelors Degree paired with three or more years of sales experience selling to a highly educated/high profile customer base. The ability to sell in an operating room, lab & hospital environment is required. A valid driver's license issued in one of the 50 States with a clean driving record is required. The ability to travel as necessary, which may include overnight and/or weekends, is required. Medical device sales experience is preferred paired with documented sales results. Individuals must live within the current geography or be willing to relocate to it. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| BD (Becton, Dickinson and Company) |
Sumter |
SC |
11/20/2009
|
| Lead Technical Associate |
| See above |
| BD (Becton, Dickinson and Company) |
Sumter |
SC |
11/20/2009
|
| Lead Business Unit Coordinator |
| See above |
| BD (Becton, Dickinson and Company) |
Sumter |
SC |
11/20/2009
|
| Lead Technical Associate |
| See above |
| BD (Becton, Dickinson and Company) |
Sumter |
SC |
11/20/2009
|
| Sr. Cost Analyst |
| See above |
| BD (Becton, Dickinson and Company) |
Sumter |
SC |
11/20/2009
|
| Production Mechanic |
| See above |
| BD (Becton, Dickinson and Company) |
Sumter |
SC |
11/20/2009
|
| Production Supervisor |
| See above |
| BD (Becton, Dickinson and Company) |
Sumter |
SC |
11/20/2009
|
| Technical Associate |
| See above |
| BD (Becton, Dickinson and Company) |
Sumter |
SC |
11/20/2009
|
| Technical Associate |
| See above |
| BD (Becton, Dickinson and Company) |
Sumter |
SC |
11/20/2009
|
| Technical Associate |
| See above |
| BD (Becton, Dickinson and Company) |
Sumter |
SC |
11/20/2009
|
| Technical Associate |
| See above |
| Johnson & Johnson Family of Companies |
Providence |
RI |
11/19/2009
|
| Providence, RI: Clinical Sales Representative: Ethicon Products, Unit of Ethicon Inc. |
| To be considered for this role, candidates must meet the following criteria: A minimum of a Bachelor's degree, at least two years of outside selling experience, excellent written and oral communication skills, a valid driver's license and clean driving record, the ability to travel as necessary (potentially overnight and/or weekend) is required. The ability to work in a lab or an operating room environment is also required. It is preferred that candidates have documented successful sales performance (high growth, results vs. plan). Be a self-starter with strong time management and planning skills, have the ability to target accounts and achieve results through a daily action plan, and be able to collaborate with other J&J associates (peers, marketing, Strategic Account Managers), external companies (distributors) and KOL's. Operating room medical device sales experience is preferred but not required. If you want to explore the many small-company environments behind the big company impact of the Johnson & Johnson Family of companies, bid on this position today |
| Johnson & Johnson Family of Companies |
Providence |
RI |
11/19/2009
|
| Providence, RI: Hernia Sales Representative: Ethicon Products, Unit of Ethicon Inc. |
| To be considered for this role, candidates must meet the following criteria: Excellent written and oral communication skills, a Bachelor's degree, valid driver's license issued in one of the 50 States and clean driving record, 3+ years experience in field sales, preferably medical device and/or capital equipment. Operating room/surgical sales experience strongly preferred. Documented successful sales performance (high growth, results vs. plan). Experience in product sales to a highly educated / high profile customer base. Ability to target accounts and achieve results through a daily action plan. Ability to travel as necessary or required, which may include overnight and/or weekend travel. If you want to explore the many small-company environments behind the big company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Providence |
RI |
11/19/2009
|
| E.Massachusetts/Rhode Island: Territory Manager: Animas Corporation |
| To be considered for this role, candidates must meet the following criteria: Minimum of a Bachelor's Degree. 4+ years of healthcare related sales experience and 2+ years medical device sales experience is preferred. Candidates must have a valid driver's license issued in one of the 50 United States and a clean driving record. Ability to demonstrate having consistently exceeded objectives in prior positions is required. The ability to travel related to this role is required. An intimate, passionate knowledge of diabetes is preferred. Solid computer skills are required. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Merck & Co., Inc. |
Montreal (West Island) |
QC |
11/19/2009
|
| Researcher in Chemistry (BS.c/MS.c level), Temporary position 12 months |
| Education and experience: We are looking for a chemist with an B.Sc /M. Sc. degree in synthetic organic chemistry with a demonstrated skill set (publications, presentations) and who is a creative analytical thinker and has a keen interest to apply his/her talents to discover new drug molecules. The chosen candidate must be prepared to join a multidisciplinary team and be involved in the entire drug discovery process. Personal research efforts are also encouraged and applicants should demonstrate interest to contribute to their field. Organic synthetic experience in the field of anti-infectious agents will be considered an asset. Language requirements: Good English communication skills (oral and written) are required. Bilingualism, English & French would be an asset. |
| Merck & Co., Inc. |
Montreal (West Island) |
QC |
11/19/2009
|
| Researcher in Process Chemistry (Ph.D.), temporary mandate 12 months |
| Education and experience: We are looking for a chemist with an Ph. D. degree in synthetic organic chemistry with a demonstrated skill set (publications, presentations) and who is a creative analytical thinker and has a keen interest to apply his/her talents to the discovery process for new drug molecules. The chosen candidate must be prepared to join a multidisciplinary team and be involved in the entire drug discovery process. Organic synthetic experience in the field of anti-infectious agents will be considered an asset. Ideally the candidate will have completed post doctoral studies and have a minimum of 2 years industrial experience.Language requirements: Good English communication skills (oral and written) are required. Bilingualism, English & French would be an asset. |
| International Partnership for Microbicides, Inc. |
|
Paarl |
11/20/2009
|
| Clinical Medical Director |
| Education/Experience
- Degree in Medicine from a tertiary institute and medical specialty preferred;
- Minimum of 10 years in clinical research environment or relevant setting;
- Minimum 5 years in pharmaceutical industry clinical research, pharmacovigilance or Medical Affairs or equivalent;
- Registration with the relevant Medical Council;
- Previous experience in the safety field and/or pharmaceutical industry;
- Experience in Clinical Medicine and Familiarity with Ethical Practices.
Knowledge, Skills, and Abilities
- Must have knowledge of Pharmacovigilance, clinical safety regulations and guidelines, and clinical research trials methodology, design, implementation and analysis;
- Must have knowledge of FDA Regulations, EMEA Regulations, ICH GCP guidelines, Local Regulations of the country where trials are being conducted, and clinical trials research and management;
- Knowledgeable and skilled in medicine and pharmaceutical product safety;
- Experience applying medical knowledge to the interpretation of individual case review;
- Experience with reporting of individual adverse events;
- Have the ability to comprehend, integrate and interpret scientific and medical data from a variety of resources;
- Experience working in a team environment, including supporting other team members when necessary promote collegiality and teamwork among peers;
- Ability think clearly and decisively and present independent, reasoned solutions to identified safety issues, helps to drive consensus of opinion, and catalyzes action to meet critical regulatory objectives;
- Demonstrated creative problem solving skills that enact change and drive continuous improvement;
- Seeks to develop self and others;
- Excellent oral, and written skills;
- Excellent communication, interpersonal and time management skills;
- Demonstrated flexibility and adaptability in a rapidly changing environment;
- Ability to build and manage inter-relationships by motivating and inspiring others.
Terms and ConditionsThis position is based in the Clinical Affairs Department in South Africa IPM office. Job holder should expect fast-paced working environment. International Travel required (at least 50%). A valid driver's license and own reliable vehicle is required. |
| International Partnership for Microbicides, Inc. |
|
Paarl |
11/20/2009
|
| Site Development Manager |
| Education/Experience
- Bachelors degree in life science or healthcare field, or equivalent;
- Minimum of five (5) yearsâ?? experience in clinical research;
- Good knowledge of regulatory and ICH/GCP guidelines required;
- Willingness and ability to travel as required (typically requires 50% travel);
- Ability to motivate and mentor, maintain positive interpersonal relationships;
- Familiarity with HIV/AIDS and/or Africa/Asia medical settings is desired;
- End-user computer efficiency, with proficiency in Microsoft Office products.
Knowledge, Skills, and Abilities
- Demonstrated poise and maturity in communicating with high-level executives;
- Excellent time management skills. Demonstrated ability to organize and prioritize multiple projects and tasks;
- Initiative - highly motivated and team oriented, but also able to work independently, assessing priorities and competently handling a variety of activities with a high degree of accuracy in a deadline-driven environment;
- Strong written and verbal communication skills; must be able to communicate effectively;
- Superior attention to detail â?? is thorough when performing work and conscientious about every aspect of work;
- Results orientation - ability to work in a fast-paced environment and meet deadlines with competing priorities.
- Demonstrated proficiency in Microsoft Office products, including Word, PowerPoint and Excel, as well as web-based research and information collection skills required.
This position is based in the Clinical Affairs Department in South Africa IPM office. Job holder should expect fast-paced working environment. |
| International Partnership for Microbicides, Inc. |
|
Paarl |
11/20/2009
|
| Medical Writer |
| Education/Experience
- Relevant tertiary education.
- Proven experience in medical and regulatory writing and editing.
- Experience with regulatory documents for a pharmaceutical company or clinical research organization.
- Must be familiar and up-to-date on regulations such as ICH guidelines and current good clinical practices.
- Must have experience and significant participation in preparation of clinical documents for regulatory submissions
- Experience in incorporating diverse feedback into a high quality document.
Knowledge, Skills, and Abilities
- Exceptional attention to detail
- Excellent verbal and written communication skills
- Demonstrated expertise with grammar, syntax, and format
- Systematic, methodical and process driven
- Ability to work precisely according to procedures, rules and regulations
- Ability to approach issues from a number of perspectives, summarizing data to draw a conclusion.
- Ability to work unsupervised taking responsibility for own actions
- Proficiency in word processing systems, i.e., Microsoft Word, MS Office or similar systems.
This position is based in the Clinical Affairs Department in Paarl, South Africa. Job holder should expect fast-paced working environment. |
| International Partnership for Microbicides, Inc. |
|
Paarl |
11/20/2009
|
| Site Development Coordinator |
| Education/Experience
- Bachelors degree in life science or healthcare field, or equivalent;
- Minimum of three (3) years experience in clinical research;
- Good knowledge of regulatory and ICH/GCP guidelines required;
- End-user computer efficiency, with proficiency.
Knowledge, Skills and Abilities
- Demonstrated proficiency in Microsoft Office products, including Word, PowerPoint and Excel, as well as web-based research and information collection skills required;
- Demonstrated poise and maturity in communicating with high-level executives.
- Excellent time management skills. Demonstrated ability to organize and prioritize multiple projects and tasks.
- Initiative-highly motivated and team oriented, but also able to work independently, assessing priorities and completely handling a variety of activities with a high degree of accuracy in a deadline-driven environment.
- Strong written and verbal communication skills; must be able to communicate effectively.
- Superior attention to detail- is thorough when performing work and conscientious about every aspect of work.
- Results orientation- ability to work in a fast-paced environment and meet deadlines priorities.
Terms and ConditionsInternational travel required (60%). Position is based in Paarl, South Africa. |
| International Partnership for Microbicides, Inc. |
|
Paarl |
11/20/2009
|
| Laboratory Monitor |
| Education/Experience
- Minimum of a Biotechnology degree or equivalent;
- Minimum of 3 yearsâ?? experience in clinical research and laboratory setting will be a preference;
- Good knowledge of Good Laboratory Practice (GCP) will be a preference;
- Experience working in an accredited laboratory;
- Experience in SOP writing;
- Willingness and ability to travel as required (typically requires 60% travel);
- Ability to motivate and mentor, maintain positive interpersonal relationships;
- Familiarity with HIV/AIDS and/or Africa medical settings is desired.
Knowledge, Skills and Abilities
- Demonstrated proficiency in Microsoft Office products, including Word, PowerPoint and Excel, as well as web-based research and information collection skills required.
- Excellent time management skills. Demonstrated ability to organize and prioritize multiple projects and tasks.
- Initiative - highly motivated and team oriented, but also able to work independently, assessing priorities and competently handling a variety of activities with a high degree of accuracy in a deadline-driven environment.
- Strong written and verbal communication skills; must be able to communicate effectively.
- Superior attention to detail â?? is thorough when performing work and conscientious about every aspect of work.
- Results orientation - ability to work in a fast-paced environment and meet deadlines with competing priorities.
Terms and ConditionsThis position is based in the Clinical Affairs Department in Paarl, South Africa. Job holder should expect fast-paced working environment. International travel required (60%). |
| International Partnership for Microbicides, Inc. |
|
Paarl |
11/20/2009
|
| Community Engagement Director |
| Education/Experience
- A Masterâ??s degree or higher in health education, community development, public health or related field is required for this position.
- Extensive experience in international and national community education, project management and stakeholder engagement.
Knowledge, Skills, and Abilities
- Strong team leadership, strategic planning, problem solving and conflict resolution skills.
- Demonstrated ability to work with diverse communities and exhibit cultural sensitivity.
- Familiarity with and sensitivity to perspectives and concerns among HIV-affected communities. Fundamental working knowledge regarding the scientific, ethical and other aspects of microbicide evaluation will be an advantage.
- Ability to communicate successfully with a variety of constituencies, including professional and clinical staff in national and international organizations, senior government officials and researchers, as well as community leaders and trial participants.
- Understanding of issues and organizational structure of HIV prevention and services at the community level.
- End-user computer efficiency, with proficiency in Microsoft Office products.
- Ability to motivate and influence others, and maintain positive interpersonal relationships;
- Ability to organize and prioritize multiple projects and tasks.
- Excellent verbal and written skills; must be able to communicate effectively at all levels of the organization.
- Ability to work independently and in a cross-functional and cross cultural team environment;
- Good conflict resolution and problem solving skills.
This position is based in the Clinical Affairs Department in Paarl, South Africa. Job holder should expect fast-paced working environment. International Travel required (at least 50%). |
| Morphotek®, Inc. |
Exton |
PA |
11/19/2009
|
| Training Administrator |
| Knowledge/Skills/Abilities Required
BA/BS in Business Administration, Human Resources, or a related field required.
2-3 years training, career counseling, career development or related experience in the biotechnology or pharmaceutical industry required.
Previous experience designing, delivering and/or implementing training programs required.
Experience in Learning Management Systems (LMS) and solid understanding of training operations required.
Advanced proficiency in MS Office applications required.
Excellent organizational, written communication, verbal communication, facilitation, presentation and interpersonal skills required.
Proven ability to work independently required.
Occasional travel may be required. |
| Johnson & Johnson Family of Companies |
Philadelphia |
PA |
11/19/2009
|
| State College, PA:- Professional Sales Specialist - LifeScan, Inc. |
| This position requires a 4 year degree, as well as, a minimum of 2 years of outside sales experience preferred. 3-5 years of sales experience in a healthcare professional sales environment or experience in professional diabetes care or related healthcare fields strongly preferred. Candidates must have a valid driver's license issued in one of the 50 United States and a clean driving record. This position may require overnight and/or weekend travel. Excellent written and oral communication skills are essential. Preference will be given to candidates living within 30 miles of the territory, with documented history of proven sales success in outside sales, pharmaceutical, or medical products industry. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Merck & Co., Inc. |
Upper Gwynedd |
PA |
11/19/2009
|
| Director Clinical Research, Oncology |
| · M.D or M.D./Ph.D who is Board Certified or Eligible in Oncology (and Hematology);· Must have experience in industry or academia;· Demonstrated record of scientific scholarship and achievement;· A proven track record in clinical medicine and background in biomedical research is essential;· Prior specific experience in clinical research and prior publication is desirable but not necessary; and· Strong interpersonal skills, as well as the ability to function in a team environment are essential. About MerckConsistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world.We offer an excellent salary and an industry-ranked benefits program, including tuition reimbursement, work-life balance initiatives and developmental programs at all levels. Merck's retirement package includes a pension plan and one of the best 401(k) plans in the nation.To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # CLI001839. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations.Our work is someone's hope. Join us.Where patients come first - MerckSearch Firm RepresentativesPlease Read Carefully:Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Site Compliance Specialist |
| Education:A Bachelor of Science in a life science (such as Biology, Chemistry, etc.) or an appropriate Engineering field is required; candidates with majors in other fields will not be considered. A major in Biology, Microbiology, Biochemistry, Virology, or Engineering is preferred. Required:At least two (2) years of experience, in broad based quality control and/or quality assurance audits or inspections, or other experience in a variety of manufacturing, packaging, testing, or technical support areas. Desired:Experience in bulk vaccine manufacturing or other bulk vaccine support area is desirable. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # QUA001929. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Quality Compliance Auditor |
| Education: A Bachelor's degree is required, preferably in an appropriate scientific or engineering field. Candidates with major fields of study in other areas may be considered if they possess additional relevant experience. Required:Minimum of 1 year of experience in a manufacturing or research environment or a related field. Strong communication and leadership skills. Must be attentive to detail. Basic understanding of regulatory requirements and cGMPs. Must be able to work rotating night shift (6PM-6AM), including weekends, and to complete several months of training on first shift. Preferred:Aseptic gowning may be required. Titers may be required. Vaccine or pharmaceutical manufacturing experience. Quality control and/or quality assurance audit/inspection experience. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition #Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Principal Development Engineer |
| Education:BS, MS or PhD Degree in Chemical Engineering, Materials Engineering/Science or Pharmaceutics with a minimum of 8 years post-bachelors degree experience in Technical Operations, Process Development, or related experience (Ph.D., 4 years or more experience required). Required:At least 3 years of experience in the formulation/development and technology transfer of controlled release dosage forms. Strong Chemical Engineering skills with a desire to perform hands-on work including design and execution of experiments at both pilot scale and during scale up. Thorough understanding of polymer chemistry and other materials along with their impact on drug release. Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. We offer an excellent salary and an industry-ranked benefits program, including tuition reimbursement, work-life balance initiatives and developmental programs at all levels. Merck's retirement package includes a pension plan and one of the best 401(k) plans in the nation. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # ENG002042. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Our work is someone's hope. Join us.Where patients come first - Merck Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Manufacturing Supervisor |
| Required Education:High School or GED Preferred:B.S. with emphasis in Science or Engineering Experience RequiredMinimum 2 years working experience in cGMP or equivalent environment. Willingness to work off-shift or weekends. Computer literacy in MS Office, Word, Outlook, Excel. PreferredcGMP experience in a sterile, bulk or finished pharmaceutical environment. Supervisory experience in a heavily regulated industry (ex. FDA, Military, Nuclear, Petro-Chemical). Manufacturing plant experience in operational capacity. Experience working within a Union environment. Experience with working in SAP or other Enterprise software. Technical writing experience related to investigations in to mfg process variation. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # MAN000345. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. ZZ5ML |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Senior Manufacturing Supervisor |
| Educational Requirements:High School or GED Required Experience/Skills:Minimum 3 years of Supervisory experience. Minimum 2 years working experience in cGMP environment. Willingness to work off-shift or weekends. Computer literacy in MS Office, Word, Outlook, Excel. Preferred: Education:B.S. with emphasis in Science or Engineering. Experience:cGMP experience in a sterile, bulk or finished pharmaceutical environment. Supervisory experience in a heavily regulated industry (ex. FDA, Military, Nuclear, Petro-Chemical). Manufacturing plant experience in operational capacity. Experience working within a Union environment. Experience with working in SAP or other Enterprise software. Technical writing experience related to investigations into manufacturing process variation. Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. We offer an excellent salary and an industry-ranked benefits program, including tuition reimbursement, work-life balance initiatives and developmental programs at all levels. Merck's retirement package includes a pension plan and one of the best 401(k) plans in the nation. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # MAN000338. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. ZZ5ML |
| Johnson & Johnson Family of Companies |
Fort Washington |
PA |
11/19/2009
|
| Associate Director, Medical Affairs - Pain Innovation |
| A life science doctoral degree (MD, DO, PhD, PharmD) is required. For healthcare providers, an active unrestricted license to practice medicine is preferred. For physicians, board certification (or equivalent) is desirable. Certification in rheumatology and/or pain management is preferable. Patient care experience is required. Pharmaceutical experience and/or exposure to clinical research in an academic setting is preferred. Complimentary or alternative pain therapies experience is preferred. Clinical research and development experience, especially experience working with pain medicines and products is preferable. Expertise in pharmaceutical new product and claims development including line extensions and Rx-to-OTC switches is preferred? Strong leadership and interpersonal skills are required. Motivated, self-starting team player with the leadership qualities needed to participate on global cross-functional teams is required. Analytical and presentation skills that facilitate translating scientific/medical/technical concepts to non-scientists clearly and concisely is required. Strong oral and written English skills are required. This position is based in Fort Washington, PA and requires 10% domestic and international travel. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Supplier QA Data Management Coordinator |
| Education:BS/BA degree in an Engineering, Science, or Business field. Required:Minimum 5 years experience in commercial, business, quality, technical or manufacturing operations functions. Familiarity with regulatory requirements that govern GMPs (e.g. CFR and Eudralex) Experience writing SOPs, Policies, and/or Guidelines. Ability to use Microsoft Excel to enter data and use formulas to calculate information. Experience developing PowerPoint slides and delivering presentations to management. Excellent analytical and computer skills, including software packages used in the maintenance and analysis of data. Excellent interpersonal and communications skills. Ability to work independently with all levels of the organization along with strong planning/organization skills. Preferred:Experience using Lean Six Sigma tools, particularly Black Belt or Green Belt certification. Familiarity with the MMD Quality Management Systems (QMS). Experience operating a database to enter, store, retrieve, and trend data and well as document management (e.g. MIDAS, Documentum, Panagon). Experience developing process flowcharts and using Microsoft Visio. Familiarity with Microsoft Project to assist in developing project plans and timelines. Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. We offer an excellent salary and an industry-ranked benefits program, including tuition reimbursement, work-life balance initiatives and developmental programs at all levels. Merck's retirement package includes a pension plan and one of the best 401(k) plans in the nation. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # QUA001933. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Our work is someone's hope. Join us.Where patients come first - Merck Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Supplier QA Relationship Manager |
| Education:BS/BA degree in an Engineering, Science, or Business field. Required:Minimum 6 years experience in commercial, business, quality, technical or manufacturing operations functions. Must have strong demonstrated interpersonal and communication skills. Must have demonstrated personal networking and relationship building skills. Ability to work independently with all levels of the organization is required. Familiarity with regulatory requirements that govern GMPs (e.g. CFR and Eudralex). Travel to supplier locations to develop and manage the supplier/Merck relationships is a key enabler of success with this position. The travel expectations are ~ 10% to 25%. Experience writing SOPs, Policies, and/or Guidelines. Ability to use Microsoft Excel to enter data and use formulas to calculate information. Experience developing PowerPoint slides and delivering presentations to management. A key responsibility of this position is to serve as the primary point of contact for coordination, oversight, problem solving and communication with MMD's suppliers. Must have tangible experiences, either internal or external to Merck, associated with relationship building and networking. Preferred:Technical writing skills, and experience with data management, collection and analysis. A strong knowledge of and broad experience in Quality Assurance. Experience in conducting or participating in atypical process investigations is preferred, as working with suppliers to resolve problems and implement corrective actions using problem solving techniques is a key expectation. Experience developing process flowcharts and using Microsoft Visio. Familiarity with the MMD Quality Management Systems (QMS). Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # QUA001949. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Staff Engineer |
| Education:· B.S in Engineering, Biological Sciences, Chemistry or Physics. M.S. in Engineering, Biological Sciences, Chemistry or Physics preferred.Required:· Minimum of 4 years work experience required; with 2 years of work experience specifically in the field of validation. Specific experience in at least one of the following areas is required:· Filter performance qualification using Filter Integrity testers, bubble point, and diffusive flow testing. Experience in validation desired; alternatively, experience in engineering or operations is acceptable with use of sterilizing filters, tangential flow filtration, ultra filtration, and vent filters.· Container/ Closure Integrity testing using microbial ingress and helium leak testing. Experience in validation desired; alternatively, experience in engineering or operations using welders, sealers, and aseptic fluid transfers using sterile bags and manifolds is acceptable.· Experience in a GMP or ISO13485 laboratory performing microbiology, environmental monitoring or engineering development work. Support the GVTE / BSV Lab Coordinator, with performing instrument qualification, metrology, SOP development , creating training material, lab notebook review, performance of internal audits (chemical hygiene, safety, 5S, GMP), and carrying out improvements activities and corrective actions in response to audits.Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition #ENG002123. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Principal Development Engineer |
| Education:BS, MS or PhD Degree in Chemical Engineering or Materials Engineering/Science. Required:A minimum of 8 years post-bachelors degree experience in Manufacturing, Process Development, or acceptable related experience (Ph.D., 4 years or more experience required). Strong Chemical Engineering skills with a desire to perform hands-on work including design and execution of experiments at various scales (lab/ pilot plant etc). Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # CHE001837. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Staff Scientist |
| Education Minimum Requirement: Bachelors Degree in microbiology, biochemistry, biochemical engineering or related field plus three years related experience. Masters Degree D in microbiology, biochemistry, biochemical engineering or related field preferred. Required Experience and Skills - Strong technical background in cell culture, molecular and microbiology, excellent communication skills, demonstrated ability to troubleshoot bioprocesses, and the ability to work in a team environment. The candidate must be experienced in aseptic technique, be able to work efficiently in a high paced environment and collaborate well with others. Desired Experience and Skills - Virology experience and Assay development. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition #ENG002118. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Research Fellow (Particle Sizing) |
| Education:PhD required Required:At least 5 years of post-doctoral or industrial experience. Candidate must demonstrate expertise and hands-on experience in the application of biophysical methodologies in characterization of biomolecules. Expertise should include theoretical and working knowledge of light scattering methodologies such as multi-angle light scattering (MALS), and varied spectroscopic techniques (CD, AUC, etc.). Qualified candidate is required to be highly motivated and possessing excellent verbal communication and writing skills. The candidate is expected to maintain a high degree of scientific rigor under all circumstances and be accessible to provide scientific supervision. The candidate must also demonstrate ability to work effectively both independently and in a multidisciplinary team environment. The individual can be expected to represent the department at cross-functional team meetings in support of data or decisions arising thereof. Preferred:Experience in innovative solutions to biological particle manipulation, aggregation source, molecular size determination and stabilization over a wide size range of biologics (proteins to viruses). GLP/GMP experience. Significant pharmaceutical experience. Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. We offer an excellent salary and an industry-ranked benefits program, including tuition reimbursement, work-life balance initiatives and developmental programs at all levels. Merck's retirement package includes a pension plan and one of the best 401(k) plans in the nation. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # BIO002487. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Our work is someone's hope. Join us.Where patients come first - Merck Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Morphotek®, Inc. |
Exton |
PA |
11/19/2009
|
| Associate Director, Technical Quality Operations |
| Job Requirements and Qualifications
Education: Graduate level degree in biological sciences or related subjects. Ph.D. preferred
Knowledge Requirements:
Knowledge of protein chromatography, mammalian cell culture and expression systems
Strong working knowledge of cGMP
Excellent written and verbal communication
Excellent interpersonal skills required, in addition to analytical problem solving, the ability to set priorities and achieve goals, and strategic thinking
Ability to manage multiple projects
Willingness and ability to assist all team members to achieve project goals
Working knowledge of Microsoft Office (Word, Excel, and Access).
Technical writing
Experience:
Minimum 10 years experience with cell culture, microbial fermentation and purification processes, scale up strategies and analytical testing of biologics, with at least 1-2 years of antibody manufacturing experience in an FDA regulated environment. Experience performing Quality Assurance functions such as SOP and protocol writing, batch record review, and investigations into deviations and out of specification results is highly preferred.
Other Information
Special Information (Travel required, physical requirements, on-call schedules, and etc.):
Travel 20-30%
Normal office environment
Laboratories on Site: Use of lab coat and safety goggles, as applicable
|
| Merck & Co., Inc. |
West Point, United States |
PA |
11/19/2009
|
| Process Engineer |
| Education:BS in chemical/biochemical engineering, pharmaceutical science or chemistry/biology. MS in chemical/biochemical engineering, pharmaceutical science or chemistry/biologyRequired:3 years manufacturing experience in the areas of pharmaceutical process start up and technical transfer or have demonstrated experience in these areas.Must be able to multi-task and work within tight deadlines. This position requires flexibility and the ability to work independently, as well as excellent organizational skills. Strong professional and interpersonal communication skills are also required. Travel will be a requirement of this position at approximately 30% (US, Puerto Rico, and China). Preferred:Experience with packaging operations is desired. The individual should also possess strong business acumen and interpersonal skills.Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # CHE002152. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm Representatives Please Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Co-op- Sterile Manufacturing |
| This position requires applicants to be pursing degree (BS/MS) in Engineering, Science, or operations based Business degrees (Industrial Engineering or Commerce and Engineering).Grade Point Average (GPA) of at least 3.0 or higher is preferred. Applicants must be available for full-time employment for 6 months with targeted start date in March 2010. Ideal candidate will be currently enrolled in an academic program and returning to school following this assignment. Successful candidate will possess strong interpersonal skills and writing skills, with an attention to detail. Previous experience in the pharmaceutical industry is preferred but is not a requirement. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition #ADM004024. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Co-op- Viral Vaccine Engineering Services |
| This position requires applicants to be pursuing degree in Chemical, Mechanical, or related Engineering discipline. A Grade Point Average (GPA) of at least 3.0 is preferred. Candidate must be available for full time employment (40 hours per week) for a period of 6 months targeted to begin in March 2010. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities" create a profile and submit your resume for requisition #ADM004026. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Co-op Global Vaccine Technology & Engineering |
| This position requires applicants to be pursuing degree in Chemical or related Engineering discipline, with a focus on technical support or related field. A Grade Point Average (GPA) of at least 3.0 is preferred. Candidate must be available for full time employment (40 hours per week) for a period of 6 months targeted to begin in March 2010. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities" create a profile and submit your resume for requisition #ADM004028. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Morphotek®, Inc. |
Exton |
PA |
11/20/2009
|
| Scientist, Bioanalytical Development |
| Knowledge/Skills/Abilities Required
• BS/MS with 5-7 yrs or PhD with 0-2 yrs relevant experience required.
• In-depth knowledge and understanding of bioanalytical assays for protein macromolecules with strong scientific and technical skills in method development and validation.
• A minimum of 5 years of hands-on experience in the development and/or validation of quantitative ligand binding and immunogenicity assays for biologics (e.g. antibodies, proteins or peptides).
• Well versed in current regulatory guidance and industry practices for development and validation of bioanalytical methods for large molecule biologics.
• Excellent verbal and written communication skills.
• Experience in GLP and/or clinical regulatory compliance is desired.
• Strong analytical skills, and a demonstrated ability to work both independently and in a team setting required.
|
| Johnson & Johnson Family of Companies |
Philadelphia |
PA |
11/19/2009
|
| Philadelphia, PA: Alternate Care Sales Representative: Ethicon Products, Unit of Ethicon Inc |
| To be considered for this role, candidates must meet the following criteria: A minimum of a Bachelor's degree, at least three years of outside selling experience, excellent written and oral communication skills, a valid driver's license and clean driving record, the ability to travel as necessary (potentially overnight and/or weekend) is required. The ability to work in a lab or an operating room environment is also required. It is preferred that candidates have documented successful sales performance (high growth, results vs. plan). Be a self-starter with strong time management and planning skills, have the ability to target accounts and achieve results through a daily action plan, and be able to collaborate with other J&J associates (peers, marketing, Strategic Account Managers), external companies (distributors) and KOL's. Suture Sales experience and Distribution Sales is highly preferred but not required. If you want to explore the many small-company environments behind the big company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Merck Manufacturing Business Intern |
| This position requires applicant to be currently working toward a Bachelors degree in Supply Chain Management, Engineering, Business or a related discipline. Must be available for 10 week internship beginning June 2010. Candidate must be eligible to work in the U.S. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition #ADM003948. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Chemical Engineer |
| Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # CHE002008. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Process Engineer |
| Education:B.S. in Chemical Engineering or Biological Sciences plus a minimum of 5 years relevant experience. Preferr M.S./Ph.D. in Chemical Engineering or Biological Sciences with a minimum of 3 years related experience Required:Experience with CIP/SIP/process design Demonstrated leadership and teamwork skills, excellent analytical abilities, established written and verbal communication skills. Experience leading a team Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # CHE002132. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm Representatives Please Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Staff Engineer/Scientist |
| Required:BS / MS in Biological Sciences/Chemical Engineering/Biological Engineering/Chemistry with at least 2 (for BS) / 0 (for MS) years relevant experience. Has technical expertise in mammalian and/or yeast based systems. Has demonstrated ability for independent project work. Desired: Both downstream and upstream experience preferred, but in-depth experience in one area acceptable. Prior experience in late stage bulk process development, process validation, authoring regulatory BLA sections and/or working with external contract organization for development and or manufacturing is a plus. Working understanding of analytical methods to characterize biologics and /or US/EU regulatory requirements and / or working knowledge of cGMPs is a plus. Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. We offer an excellent salary and an industry-ranked benefits program, including tuition reimbursement, work-life balance initiatives and developmental programs at all levels. Merck's retirement package includes a pension plan and one of the best 401(k) plans in the nation. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition #SCI003878. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Our work is someone's hope. Join us.Where patients come first - Merck Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Quality Engineer |
| Education:Bachelor's degree required. The desired educational background is a BS in an appropriate Engineering field, Operations Improvement, or Business Administration. Other fields of study will be considered if accompanied by significant relevant experience. Required:Three or more years of related Industrial, Production, or Staff experience, obtained through post-degree work in one or more of the following areas: Project management, operations support, or process improvement Financial analysis, resource allocation, or budget / profit plan management Capital plans and/or projects Regulatory and/or compendial requirements Preferred:Experience in one or more of the following areas: Facilities / space planning Operations research techniques Vendor relations and/or contract negotiation Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # QUA002013. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Documentation Center Assistant |
| Educational requirements:High School diploma Required skills and experience:Excellent customer service, including phone and in-person communication skills. Advanced computer skills. Familiarity with databases. Strict attention to detail. Ability to follow directions exactly. Ability to work "on-call" as needed. Preferred skills and experience: Prior documentation experience (electronic and hard copy). Experience in a GMP environment. Pharmaceutical industry experience. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # ADM004036. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Release Analyst |
| EducationA Bachelor's degree is required, preferably in an appropriate scientific or engineering field. Candidates with major fields of study in other areas may be considered if they possess additional relevant experience. RequiredAt least three (3) years of relevant post-degree work experience in a manufacturing or research environment or a related field. Strong analytical, problem solving, oral and written communication skills, leadership, and attention to detail. Solid understanding of regulatory requirements and GMPs. PreferredAseptic gowning may be required. Tites may be required. Vaccine or pharmaceutical manufacturing experience. Quality control and/or quality assurance audit/inspection experience. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # REL000149. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Manufacturing Engineer |
| Educational requirements: B.S. or M.S. in Chemical or Mechanical Engineering. Required skills and experience: The position requires basic technical writing skills and strong oral communication. Minimum 1 year Aseptic or pharmaceutical manufacturing experience, technical support or quality role or equivalent. Preferred skills and experience: Minimum 3 year Aseptic or pharmaceutical manufacturing experience, technical support or quality role or equivalent. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # CHE002179. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Johnson & Johnson Family of Companies |
Wilkes Barre |
PA |
11/19/2009
|
| Scranton, PA: Sales Representative: J&J Wound Management: Biosurgicals, Unit of ETHICON, Inc. |
| To be considered for this role, candidates must meet the following criteria: A minimum of a Bachelor's degree, minimum of two years outside selling experience, the ability to travel as necessary (potentially overnight and/or weekend) is required. Must have a valid driver's license and clean driving record; and, excellent written and oral communication skills. Would prefer candidates with documented successful sales performance (high growth, results vs. plan), ability to target accounts and achieve results through a daily action plan; and ability to collaborate with other J&J associates (peers, marketing, Strategic Account Managers), external companies (distributor reps) and KOLs. Self-starters with strong time management and planning skills are a plus. Hospital-based pharmaceutical or medical device experience as well as experience in product sales to a highly educated/high profile customer base is strongly preferred, but not required. Preference will be given to those individuals living within 30 miles of the posted territory. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Quality Compliance Auditor |
| Education: A Bachelor's degree is required, preferably in an appropriate scientific or engineering field. Candidates with major fields of study in other areas may be considered if they possess additional relevant experience. Required:Minimum of 1 year of experience in a manufacturing or research environment or a related field. Strong communication and leadership skills. Must be attentive to detail. Basic understanding of regulatory requirements and cGMPs. Must be able to work rotating night shift (6PM-6AM), including weekends. Preferred:Aseptic gowning may be required. Titers may be required. Vaccine or pharmaceutical manufacturing experience. Quality control and/or quality assurance audit/inspection experience. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # REL000133. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Quality Compliance Auditor |
| Education: A Bachelor's degree is required, preferably in an appropriate scientific or engineering field. Candidates with major fields of study in other areas may be considered if they possess additional relevant experience. Required:Minimum of 1 year of experience in a manufacturing or research environment or a related field. Strong communication and leadership skills. Must be attentive to detail. Basic understanding of regulatory requirements and cGMPs. Must be able to work rotating night shift (6PM-6AM), including weekends. Preferred:Aseptic gowning may be required. Titers may be required. Vaccine or pharmaceutical manufacturing experience. Quality control and/or quality assurance audit/inspection experience. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # REL000141. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Quality Compliance Auditor |
| Education: A Bachelor's degree is required, preferably in an appropriate scientific or engineering field. Candidates with major fields of study in other areas may be considered if they possess additional relevant experience. Required:Minimum of 1 year of experience in a manufacturing or research environment or a related field. Strong communication and leadership skills. Must be attentive to detail. Basic understanding of regulatory requirements and cGMPs. Must be able to work rotating day shift (6AM-6PM), including weekends. Preferred:Aseptic gowning may be required. Titers may be required. Vaccine or pharmaceutical manufacturing experience. Quality control and/or quality assurance audit/inspection experience. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # REL000137. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Our work is someone's hope. Join us.Where patients come first - Merck Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Quality Compliance Auditor |
| Education: A Bachelor's degree is required, preferably in an appropriate scientific or engineering field. Candidates with major fields of study in other areas may be considered if they possess additional relevant experience. Required:Minimum of 1 year of experience in a manufacturing or research environment or a related field. Strong communication and leadership skills. Must be attentive to detail. Basic understanding of regulatory requirements and cGMPs. Must be able to work rotating day shift (6AM-6PM), including weekends. Preferred:Aseptic gowning may be required. Titers may be required. Vaccine or pharmaceutical manufacturing experience. Quality control and/or quality assurance audit/inspection experience. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # REL000131. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Release Coordinator |
| EducationA Bachelor's degree is required, preferably in an appropriate scientific or engineering field. Candidates with major fields of study in other areas may be considered if they possess additional relevant experience. RequiredAt least three (3) years of relevant post-degree work experience in a manufacturing or research environment or a related field. Strong analytical, problem solving, oral and written communication skills, leadership, and attention to detail. Solid understanding of regulatory requirements and GMPs. PreferredAseptic gowning may be required. Tites may be required. Vaccine or pharmaceutical manufacturing experience. Quality control and/or quality assurance audit/inspection experience. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # REL000134. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Release Associate |
| Required:B.S. degree with a technical emphasis in an appropriate scientific or engineering field. At least one year of relevant post-degree work experience in a laboratory, manufacturing, or quality position. Evidence of leadership skills coupled with good oral and written communication skills, i.e. effective presentation of concepts and ideas, as well as interpersonal and conflict resolution skills. Attention to detail, flexibility and an awareness of production and attendant quality control problems. Preferred:Familiarity with manufacturing batch records is a key skill necessary for success in this position; prior batch record experience is a strong plus. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # REL000124. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Johnson & Johnson Family of Companies |
Fort Washington |
PA |
11/19/2009
|
| Associate Director, Medical Affairs - Upper Respiratory Innovation |
| A life science doctoral degree (MD, DO, PhD, PharmD) is required. For healthcare providers, an active unrestricted license to practice medicine is preferred. For physicians, board certification (or equivalent) is desirable. Certification in allergy/clinical immunology, otolaryngology or pulmonary is preferable. Patient care experience is required. Pharmaceutical experience and/or exposure to clinical research in an academic setting is preferred. Clinical research and development experience, especially experience working with upper respiratory medicines and products or complimentary or alternative therapies is preferable. Expertise in pharmaceutical new product and claims development including line extensions and Rx-to-OTC switches is preferred. Strong leadership and interpersonal skills are required. Motivated, self-starting team player with the leadership qualities needed to participate on global cross-functional teams is required. Analytical and presentation skills that facilitate translating scientific/medical/technical concepts to non-scientists clearly and concisely is required. Strong oral and written English skills are required. This position is based in Fort Washington, PA and requires 10% domestic and international travel. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Teva Pharmaceuticals USA |
North Wales |
PA |
11/20/2009
|
| Business/Market Research Analyst |
|
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| MMD PhD Biology College Recruiting |
| · PhD Biology, Microbiology, Virology· Strong personal character and ethics· Superior Communication and Interpersonal Skills· Excellent Academic Achievement, Analytical Ability· Ability to work effectively with others as well as independently· U.S. citizen or lawful permanent resident of U.S.· Laboratory experience is preferred Opportunities exist in manufacturing areas and include opportunities in process validation and manufacturing technical areas. Opportunities are available in analytical, biological, and vaccine development. Each of these opportunities provides a challenging environment to learn and contribute. The successful candidate will be expected to carry out research on assigned problems in the above listed areas, including applied development, problem solving, process / product improvement and laboratory testing in the above listed areas. Many analytical techniques are used, including both in vivo and in vitro methods, to characterize complex biological products and systems The candidate is expected to work in a team environment and provide all essential understanding toward addressing mechanisms responsible for product safety, efficacy and stability. Responsibilities will also include the analysis and interpretation of data for problem solving and predictive purposes. A company-wide program is available to facilitate individual development planning to prepare the individual for increasing responsibility according to either technical or management tracks support career path planning. This may include movement to other divisions of Merck & Co., Inc. Those who join Merck can look for substantial early responsibility, the opportunity to develop and apply state-of-the-art technologies, chances for growth and advancement in an informal, varied work environment. Specific openings in MMD are as follows:Global Vaccines Technology and Engineering (West Point, PA, Elkton, VA) is responsible for process implementation, validation and maintenance for biological processes. Specific needs are in the Bioanalytical area which is responsible for assay development and support.At Merck we believe you can develop faster if we give you real challenges right from the onset. In MMD, we encourage you to move between functional groups so that you get hands-on experience in many aspects of our operations.If you are the kind of individual who thrives on challenge and possess the technical, leadership and business skills that are of value to our business, we invite you to apply. Please go to www.merck.com/careers and enter your profile and resume for requisition BIO002450 so that we can keep track of you through the whole recruiting process. |
| Morphotek®, Inc. |
Exton |
PA |
11/19/2009
|
| Director, Quality Assurance, Pilot Plant |
| Scope Measures
Oversight of all quality assurance functions within the pilot plant, with a total headcount of ~ 15 persons over the next three years. Considerable decision making capability with regard to ensuring quality is built into development and production processes and that all regulatory and procedural requirements are adhered to.
Knowledge/Skills/Abilities Required
Graduate level degree in quality and/or biological sciences or related subjects is preferable. BS degree required.
Must have knowledge of FDA, EMEA and JP regulations as they pertain to building design, aseptic process requirements and development of antibody-based biotherapeutics.
|
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Senior Research Chemist (Continuous Recruitment) |
| Required PhD in Chemistry or Biochemistry is required. Degree completion no later than end of 2010 required. DesiredSome relevant experience via a co-op, internship, or independent research is preferred for consideration. If you, like us, strive for excellence in all you do, consider joining our team of talented and dedicated individuals from diverse backgrounds who are united in bringing Merck's finest achievements to people around the world. Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. We offer an excellent salary and an industry-ranked benefits program, including tuition reimbursement, work-life balance initiatives and developmental programs at all levels. Merck's retirement package includes a pension plan and one of the best 401(k) plans in the nation. To be considered for this position, please visit our career site at www.merck.com/careers/university/ to create a profile and submit your resume for requisition # CHE002098. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Associate Automation Engineer |
| Education:Must have earned a Bachelor's Degree in Information Technology, Science, Engineering, or related field by December 31st, 2009 or June 30th, 2010. Preferred:A working knowledge of the regulatory requirements for pharmaceutical applications is desirable. Highly desired are skills in PLCs (AB), DCSs (DeltaV / Provox), Batch Operations (S88/S95), IT, and OEM equipment. Merck Location: West Point, Pennsylvania and local satellite offices in Pennsylvania (25 miles northwest of Philadelphia) Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # ENG002126. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Quality Compliance Auditor |
| Education: A Bachelor's degree is required, preferably in an appropriate scientific or engineering field. Candidates with major fields of study in other areas may be considered if they possess additional relevant experience. Required:Minimum of 1 year of experience in a manufacturing or research environment or a related field. Strong communication and leadership skills. Must be attentive to detail. Basic understanding of regulatory requirements and cGMPs. Must be able to work rotating day shift (6AM-6PM), including weekends. Preferred:Aseptic gowning may be required. Titers may be required. Vaccine or pharmaceutical manufacturing experience. Quality control and/or quality assurance audit/inspection experience. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # QUA001961. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Associate Automation Engineer |
| Education:Must have earned a Bachelor's Degree in Information Technology, Science, Engineering, or related field by December 31st, 2009 or June 30th, 2010. Preferred:A working knowledge of the regulatory requirements for pharmaceutical applications is desirable. Highly desired are skills in PLCs (AB), DCSs (DeltaV / Provox), Batch Operations (S88/S95), IT, and OEM equipment. Merck Location: West Point, Pennsylvania and local satellite offices in Pennsylvania (25 miles northwest of Philadelphia) Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # ENG002127. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means |
| Morphotek®, Inc. |
Exton |
PA |
11/19/2009
|
| Senior Clinical Quality Assurance Specialist |
| Job Requirements and Qualifications
BA/BS degree in biological sciences, nursing or related discipline, or equivalent experience required
Strong knowledge of government regulations, guidelines and standards for investigation of new pharmaceutical products is required
Experience in QA audits of Clinical Investigators
Experience in QA audits of Clinical documents associated with clinical trials
Experience in system/process audits
Experience in development of SOPs
Working knowledge and understanding of drug development and global clinical regulatory environment
Ability to manage multiple projects
Effective organizational skills
Effective team player and detail oriented
Strong attention to detail, good organizational skills, ability to work independently
Solid oral and written communication skills with ability to communicate effectively and professionally with medical personnel
Knowledge Requirements:
Knowledge of the code of federal regulations, European Directives, ICH/GCP practices. The candidate will also have a working knowledge of clinical auditing processes. Previous participation in regulatory inspections is a plus.
Experience:
A minimum of 3-5 years working experience as a clinical quality assurance auditor.
Other Information
Special Information (Travel required, physical requirements, on-call schedules, and etc.):
Travel 25-35%
|
| Biogen Idec, Inc. |
Pittsburgh |
PA |
11/20/2009
|
| Area Business Manager, Neurology - Pittsburgh S., PA |
| Minimum 5+ years pharmaceutical sales or biotech sales experience required. Experience with reimbursement issues, product launch, and injectable/infusion product selling experience desired. |
| Johnson & Johnson Family of Companies |
|
PA |
11/19/2009
|
| Director, Medical Affairs Strategic Trials Team (Horsham, PA) |
| MD/DO or PhD with advanced management training or experience is required, preferably in Gastroenterology, Rheumatology or Dermatology. A minimum of 5 years of clinical and managerial experience in pharmaceutical trial design and conduct (Phase II-IV) is strongly preferred. Significant experience in supervising and managing clinical research programs is required. Excellent interpersonal and public speaking skills are required for this high visibility position. Demonstrated ability to work in a matrix type environment with interaction with cross-functional teams. Up to 10% travel (domestic and international) is required for this position. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Teva Pharmaceuticals USA |
Horsham |
PA |
11/20/2009
|
| Employment Law Counsel |
|
| Teva Pharmaceuticals USA |
North Wales |
PA |
11/20/2009
|
| Staffing Partner |
|
| Teva Pharmaceuticals USA |
North Wales |
PA |
11/20/2009
|
| HR Analyst |
|
| Teva Pharmaceuticals USA |
Horsham |
PA |
11/20/2009
|
| Sr Director, Clinical Reg Affairs- Women's Health |
|
| Teva Pharmaceuticals USA |
North Wales |
PA |
11/20/2009
|
| Sr. Manager, Network Administration & IT Security |
|
| Teva Pharmaceuticals USA |
North Wales |
PA |
11/20/2009
|
| Talent Development Specialist |
|
| sanofi pasteur |
Swiftwater |
PA |
11/19/2009
|
| Manager, Manufacturing Staff US |
| BS degree in Life Sciences or Engineering with relevant experience in manufacturing of biological products. 3-5 years experience in manufacturing and/or development departments. Working knowledge of cGMP's. Must have knowledge of continuous improvement techniques and problem solving skills. Excellent verbal and written communication skills. Working knowledge of SAP, validation and analytical experience is preferred. Candidate must be able to work overtime and flexible hours, including weekends. |
| sanofi pasteur |
Swiftwater |
PA |
11/19/2009
|
| Manager, Process Integration US |
| Bachelors Degree in a Life Science. 5-10 years Pharmaceutical/Biological laboratory experience in a GMP compliant Quality Control laboratory, including previous management experience. Proven team collaboration experience is essential with a focus on customer service. |
| sanofi pasteur |
Swiftwater |
PA |
11/19/2009
|
| Manufacturing Tech V |
| BS Degree in a related field and 2 - 4 years experience preferred or 10 years or more equivalent work experience. Trackwise, SAP and deviation experience a plus. |
| Morphotek®, Inc. |
Exton |
PA |
11/19/2009
|
| Associate Director, Aseptic Fill Finish Operations |
| Knowledge/Skills/Abilities Required
Strong knowledge of aseptic manufacturing of biologics as well as ICH, cGMP, EMEA and JP guidelines as they pertain to the manufacturing of monoclonal antibody based therapies required.
Minimum 8 years of relevant aseptic manufacturing experience with biologics, several of which must be in a management position required. Graduate level degree in biological sciences or related subject highly preferred. Individuals without a graduate degree but more experience will be considered.
Prior contract manufacturing project management experience is highly preferred. Prior experience with manufacturing from pre-IND through phase 3 or commercial production is highly desired.
An understanding of project accounting and financial concepts required.
A hands-on, proactive stance is essential with willingness and ability to assist all team members to achieve corporate goals required.
Up to 20% domestic and international travel required. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Senior Chemical Engineer |
| This position requires candidate to be currently enrolled in a PhD program in Chemical Engineering, Biochemical Engineering, BioMedical Engineering (process option), Bioengineering, or related field. Ideal candidate will possess superior communication and interpersonal skills. Must be graduating between August 2009 and August 2010. Candidates must be eligible to work in the US without sponsorship. Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # CHE002024. |
| Johnson & Johnson Family of Companies |
Fort Washington |
PA |
11/19/2009
|
| Product Director - Global Strategic Marketing (Ft. Washington, PA) |
| A minimum of a Bachelor's degree is required. An MBA is strongly preferred. A minimum of 5 years progressive Marketing experience in Consumer Packaged Goods is required. Over-the-Counter (OTC) industry is preferred. Experience developing and implementing successful business plans and those demonstrating the ability to turn consumer insights into new products and/or claims is required. Prior global experience is preferred. Ability to influence multiple stakeholders across multiple disciplines, geographies, and organizational levels is required. Experience identifying and driving strategy across multiple business conditions is preferred. Flexibility and ability to adapt to change and to operate effectively in ambiguous situations is required. Strong bias to action and proven track record of delivering results is required. Superior collaboration skills and the ability to create and lead high-performing cross-functional and cross-cultural teams are preferred. Intellectual curiosity and an ability to operate in a global mindset are preferred. Position requires 10-20% domestic and international travel. |
| Morphotek®, Inc. |
Exton |
PA |
11/19/2009
|
| Director, Analytical Outsourcing Program Management |
| Graduate level degree in biological sciences or related subject required. Ph.D. highly preferred with equivalent expertise required.
Must have a minimum of 8 years of relevant analytical experience with biologics, several of which must be in a management position.
Strong knowledge of biologics manufacturing and analytical methodology as well as ICH, cGMP, EMEA and JP guidelines as they pertain to the manufacturing of monoclonal antibody based therapies required.
Prior contract manufacturing project management experience is highly preferred. Prior experience with manufacturing from pre-IND through phase 3 or commercial production is highly desired.
An understanding of project accounting and financial concepts is also required since this individual will participate in budgeting, tracking and financial decision making for multiple drug development programs.
A hands-on, proactive stance is essential with willingness and ability to assist all team members to achieve corporate goals.
Excellent interpersonal skills are mandatory, in addition to analytical problem solving, the ability to set priorities and achieve goals; strategic thinking, energy, enthusiasm and an entrepreneurial mindset.
The ability and willingness to travel (domestic and international) approximately 20% of the time is required. |
| Morphotek®, Inc. |
Exton |
PA |
11/19/2009
|
| Sr. Scientist - Pharmacology |
| Job Requirements and Qualifications
Education: PhD with training in pathology, cell biology or related fields, expertise in oncology preferred but not required.
Must have at least 5 years experience in biotech/pharmaceutical industry.
Strong experimental skills in human disease model development, mammalian tissue culture, vector transduction and imaging-related technology.
Oncology experience is preferred. Experience in IHC is a plus.
A thorough understanding of molecular oncology and immunology.
Demonstrated experience in in vivo human disease model and an excellent publication record.
Supervisory experience preferred.
Excellent organizational, time management, communication, and interpersonal skills.
Strong oral and written skills, and experience maintaining a record of studies in the form of notebooks, technical reports, summaries, protocols, and quantitative analyses.
Other Information
Special Information (Travel required, physical requirements, on-call schedules, and etc.):
Some travel may be required.
|
| Johnson & Johnson Family of Companies |
Philadelphia |
PA |
11/19/2009
|
| PA/OH/WV/MD: Territory Manager: Veridex, LLC, a Division of Ortho-Clinical Diagnostics, Inc. |
| To be considered for this role, candidates must meet the following criteria: A minimum of a BA/BS degree paired with a minimum of 5-10 years of related experience strongly preferred. MBA a plus. Diagnostic field sales experience with an emphasis in the field of oncology and histopathology and technology selling preferred. Advanced knowledge of customer lymph node processes, along with a working knowledge of the appropriate supporting products a plus. Clinical Experience or related activities a plus. Knowledge of Microsoft Word, Excel, Power Point and Outlook required. Valid drivers license issued in one of the 50 States and clean driving record required. Ability to work in an operating room setting. Ability to travel as necessary or required, which may include overnight and/or weekend travel. Excellent written and oral communication skills. Self directed and self motivated, with a proven track record of career success. Ideal candidate will live (or be willing to relocate) in close proximity to a major airport. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Fort Washington |
PA |
11/19/2009
|
| Associate Director, Clinical Studies |
| A Doctoral degree in psychology, public health, outcomes research, or related scientific discipline is required. A minimum of 4 years of clinical and/or outcomes research experience including claims, clinician-rating, self-report, and/or biometric measures is required. Expertise in behavioral approaches/therapies within wellness and prevention is preferred. Hands-on statistical analysis skills using SPSS and/or SAS, including multivariate modeling is preferred. Excellent written and oral communication skills are required. Experience with publication record including data-based publications, poster and/or podium presentations at scientific conferences is required. Evidence of strong innovation skills preferred. |
| Johnson & Johnson Family of Companies |
|
PA |
11/19/2009
|
| Principal Research Scientist (Data Warehouse Administrator) - Radnor |
| A minimum of a PhD is required with at least 5 years of experience. Knowledge of biology and/or clinical science in the therapeutic areas of interest (immunology, oncology, etc.) is required. Must have excellent communication skills, demonstrated leadership skills, and the ability to operate in matrixed and global environment. Technical expertise with bioinformatics and/or medical informatics applications is required. Must have experience with database development in commercial setting as well as experience with data mining algorithms and applying them to biological and/or clinical problems. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Fort Washington |
PA |
11/19/2009
|
| 2010 MBA Marketing Summer Intern, PA |
| Graduate student pursuing a MBA or Master's degree (concentration in Brand Management or Marketing is preferred). You must be enrolled in an MBA or other business-related graduate program and planning to obtain your degree in or before July 2011. Candidate must possess excellent creative instincts and strong leadership skills. Candidate must have permanent work authorization in the U.S. Candidate must be willing to in Fort Washington, PA. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Admin Assist 14 Step 14-16-18 |
| Education:· High School Diploma or G.E.D. Required:· 1-3 years Secretarial experience· Must successfully pass the applicable skills/aptitude assessment· Core skills in word processing software (e.g. Microsoft Word)· Core skills in e-mail/calendar/scheduling software (e.g. Microsoft Outlook)· Core skills in presentation software (e.g. Microsoft PowerPoint)· Core skills in spreadsheet software (e.g. Microsoft Excel) Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # MER000117. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Manufacturing Supervisor |
| Please note that this positon is a rotating shift position: 12 Hour Rotating Shift(2 Days on - 2 Days Off then 5 days on)Hours will be 6 AM - 6PM and/or 6PM - 6AM Qualifications (Required): Manufacturing SupervisorEducation:High School or GED Experience/Skills:Minimum 2 years working experience in cGMP or equivalent environment Willingness to work off-shift or weekends Computer literacy in MS Office, Word, Outlook, Excel Qualification (Preferred):Manufacturing Supervisor Education:B.S. with emphasis in Science or Engineering Experience cGMP experience in a sterile, bulk or finished pharmaceutical environment. Supervisory experience in a heavily regulated industry (ex. FDA, Military, Nuclear, Petro-Chemical) Manufacturing plant experience in operational capacity Experience working within a Union environment Experience with working in SAP or other Enterprise software Technical writing experience related to investigations in to mfg process variation Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # MAN000327. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. ZZ5ML |
| sanofi pasteur |
Swiftwater |
PA |
11/19/2009
|
| Library & Information Access Intern |
| - College science background in Biology or Chemistry or Library/Information Science.
- Minimum overall GPA of 3.2
- Full-time, matriculating student who has completed sophomore year at an accredited college or university.
- Demonstrated leadership skills
- Excellent communication and organization skills
- Strong proficiency with MS Office applications
- Good interpersonal skills a must
- Good attention to detail
- Scientific background necessary with database experience a plus. |
| sanofi pasteur |
Swiftwater |
PA |
11/19/2009
|
| Library & Information Access Intern |
| College science background in Biology or Chemistry or Library/Information Science.
- Minimum overall GPA of 3.2
- Full-time matriculating student who has completed sophomore year at an accredited college or university
- Demonstrated leadership skills
- Excellent communication and organization skills
- Strong proficiency with MS Office applications
- Good interpersonal skills a must
- Good attention to detail
- Database, information science or library background a plus, especially cataloging. |
| sanofi pasteur |
Swiftwater |
PA |
11/19/2009
|
| Biostatistician |
| Ph.D. in Statistics or related field or equivalent experience; 3-5 years (MS. and 5-7 years) relevant pharmaceutical/vaccines industry experience.
At least 2 years experience using SAS software, especially base, statistics, and graphics.
At least 2 years experience designing clinical trials.
At least 2 years experience developing statistical analysis plans and statistical methods sections for protocols.
Demonstrated use of sample size estimation and power calculation tools/software.
Very good oral and written communication skills.
Demonstrated ability to work independently and to work in a multidisciplinary team.
Experience with non-inferiority trials, a plus.
Author or co-author of publications, a plus.
NDA, BLA, or CTD submission experience, a plus. |
| Johnson & Johnson Family of Companies |
West Chester |
PA |
11/19/2009
|
| DIRECTOR BILLING & CONTRACT COMPLIANCE |
| BA/BS degree is required, advanced degree is preferred. A minimum of ten years overall business experience with five years in biopharmaceutical, pharmaceutical, or medical device industry is required. Experience working with or familiar with DME Supplier standards is required. Experience working in government/commercial compliance, contracting including but not limited to operational experience in impact analysis and strategic overlays (Pharmaceutical, Device and/or Consumer) and timely/accurate remediation and adjudication, law or related area is required. Experience supervising projects using internal and/or external resources within a matrix environment is required. Demonstrated experience with HCC and GCC programs is required. Health Care Compliance certifications are preferred. This position will be based in West Chester, Pa and will require 15% travel. Due to technical upgrades, this requisition is replacing requisition #0903460. Any candidates who have already applied to requisition #0903460 are already being considered, therefore, you do not need to apply. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Lead, Learning & Behavior Realization |
| Educational Requirements: Minimum of five years in a highly regulated industry (preferably pharmaceutical). BS/BA degree in education, science or engineering. Required experience and skills:Minimum of four years experience in instructional design/technology, organizational development, or performance consulting. Excellent communication skills Ability to facilitate cross-functional teams. Ability to collaborate with others. Self-motivated and adaptable Ability to plan and organize work. Ability to learn, understand and communicate business needs and solutions. Ability to solve problems creatively. Computer Skills Ability to drive results. Ability to think strategically. Ability to influence stakeholders. Ability to leverage diversity. Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. We offer an excellent salary and an industry-ranked benefits program, including tuition reimbursement, work-life balance initiatives and developmental programs at all levels. Merck's retirement package includes a pension plan and one of the best 401(k) plans in the nation. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition #EMP000210 . Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Our work is someone's hope. Join us.Where patients come first - Merck |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Staff Biochemist |
| Education Minimum Requirement: Master's Degree or a Bachelor's degree with a minimum 2 years of industry experience Required Experience and Skills: Experience with mammalian cell culture and cell-based potency assays, both on a large scale Basic knowledge of MS Word and Excel Desired Experience and Skills: Experience with automation, ie Backman instrumentation Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # BIO002470. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Gen. Techn.-Sheet Metal Worker |
| Education: High School Diploma or equivalent required. Graduation from a recognized sheet metal trade school, OR the completion of a formal sheet metal worker apprectice program. Requirements: At least three years recent full-time experience as a journeyman sheet metal worker, OR the recent completion of four years' on the job training as part of a formal sheet metal worker apprentice program. Preferred: More than 3 years experience as a Journeyman sheet metal worker Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. We offer an excellent salary and an industry-ranked benefits program, including tuition reimbursement, work-life balance initiatives and developmental programs at all levels. Merck's retirement package includes a pension plan and one of the best 401(k) plans in the nation. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # USW000188. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Senior Engineer/Scientist |
| Education Requirement: BS/MS/PhD in Biological Sciences/Chemical Engineering/Biological Engineering/Chemistry with at least 6 years relevant experience (May be combination of post-graduate education and/or work-related experience.) Required: Has technical expertise in mammalian and/or yeast based systems. Has demonstrated ability for independent project leadership. Desired: Both downstream and upstream experience preferred, but in-depth experience in one area acceptable. Prior experience in late stage bulk process development, process validation, authoring regulatory BLA sections and/or working with external contract organization for development and or manufacturing would be preferred. Working understanding of analytical methods to characterize biologics, US/EU regulatory requirements is a plus; working knowledge of cGMPs is an added benefit. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # SCI003914. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Research Fellow |
| Education:Ph.D. degree in biochemistry, pharmaceutical sciences or a related field Required:A broad understanding of the pharmacokinetics and disposition of therapeutic proteins. 3 or more years of industrial or academic experience in DMPK support of Biologics discovery/development programs. Excellent written and verbal communication skills. Preferred:Three or more years of industrial or academic experience in pharmacokinetic/pharmacodynamic (PK/PD) modeling. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition #PHA000871. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Quality Compliance Specialist |
| Education: A Bachelor's degree is required, preferably in an appropriate scientific or engineering field. Candidates with major fields of study in other areas may be considered if they possess additional relevant experience. Required:Minimum of 3 years of experience in a manufacturing or research environment or a related field. Strong communication and leadership skills. Must be attentive to detail. Basic understanding of regulatory requirements and cGMPs. Must be able to work rotating night shift (6PM-6AM), including weekends, and to complete several months of training on first shift. Preferred:Aseptic gowning may be required. Titers may be required. Vaccine or pharmaceutical manufacturing experience. Quality control and/or quality assurance audit/inspection experience. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # QUA001974. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Environmental Monitoring Technician |
| Education:High School Diploma or equivalent. PLUS a minimum of 60 credits from an accredited university/college to include a minimum of 4 credits in Biological Science with a lab, 4 credits in Microbiology or Bacteriology with a lab, 4 credits in General Chemistry with a lab, and 3 credits in Mathematics are required. Required:Ability to lift/move up to 45 pounds Good working knowledge of aseptic techniques Willing to work in a 3rd Shift Union Position - Monday through Friday, 12am through 8:30am EST. Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. We offer an excellent salary and an industry-ranked benefits program, including tuition reimbursement, work-life balance initiatives and developmental programs at all levels. Merck's retirement package includes a pension plan and one of the best 401(k) plans in the nation. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition USW000243. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Our work is someone's hope. Join us.Where patients come first - Merck Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Environmental Monitoring Technician |
| Education:High School Diploma or equivalent. PLUS a minimum of 60 credits from an accredited university/college to include a minimum of 4 credits in Biological Science with a lab, 4 credits in Microbiology or Bacteriology with a lab, 4 credits in General Chemistry with a lab, and 3 credits in Mathematics are required. Required:Ability to lift/move up to 45 pounds Good working knowledge of aseptic techniques Willing to work in a 2nd Shift Union Position - Sunday through Thursday, 4pm to 12:30am EST. Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. We offer an excellent salary and an industry-ranked benefits program, including tuition reimbursement, work-life balance initiatives and developmental programs at all levels. Merck's retirement package includes a pension plan and one of the best 401(k) plans in the nation. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition USW000238. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Our work is someone's hope. Join us.Where patients come first - Merck Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Environmental Monitoring Technician |
| Education:High School Diploma or equivalent. PLUS a minimum of 60 credits from an accredited university/college to include a minimum of 4 credits in Biological Science with a lab, 4 credits in Microbiology or Bacteriology with a lab, 4 credits in General Chemistry with a lab, and 3 credits in Mathematics are required. Required:Ability to lift/move up to 45 pounds Good working knowledge of aseptic techniques Willing to work in a 2nd Shift Union Position - Monday through Friday, 4pm to 12:30am EST. Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. We offer an excellent salary and an industry-ranked benefits program, including tuition reimbursement, work-life balance initiatives and developmental programs at all levels. Merck's retirement package includes a pension plan and one of the best 401(k) plans in the nation. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition USW000230. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Our work is someone's hope. Join us.Where patients come first - Merck Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
West Point |
PA |
11/19/2009
|
| Process Engineer |
| Education: BS in Chemical Engineering, Bio-Engineering or Biosciences. MS in Chemical Engineering, Bio-Engineering, or Biosciences preferred. Required:Demonstrated Technical Strength. Strong Analytical Problem-Solving. Ability to lead teams. Effective Communication, both verbal and written. Strong Collaboration & Leadership experience. Preferred:GMP experience, Cell Culture and/or Virology experience. Previous Technology Transfer experience. Experience with Aseptic Processing and related equipment desired. Knowledge and experience of CIP and SIP. Knowledge or experience of six sigma methodology, process analytical technology, process monitoring and control. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # PRO007596. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm Representatives Please Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by |
| Novartis Oncology |
na |
OR |
11/20/2009
|
| Psychiatry Sales Specialist - Portland, OR FW2H2C |
| Bachelors degree (preferably in Life Sciences, Pharmacy or Business related discipline).
Minimum two years of pharmaceutical specialty sales experience.
At least one year of pharmaceutical sales experience in the institutional sector, preferably with Psychiatrists.
Familiarity with the Psychiatric community is a plus.
This position may require significant travel due to the large geography that the incumbent will be responsible for.
Must work within 50 miles of the region?s border.
Novartis is committed to embracing and leveraging diverse backgrounds, cultures and talents to achieve competitive ad-vantage. Novartis is an equal opportunity employer M/F/D/V |
| Novartis Oncology |
na |
OR |
11/20/2009
|
| Psychiatry Sales Specialist - Eugene, OR FW2H1D |
| Bachelors degree (preferably in Life Sciences, Pharmacy or Business related discipline).
Minimum two years of pharmaceutical specialty sales experience.
At least one year of pharmaceutical sales experience in the institutional sector, preferably with Psychiatrists.
Familiarity with the Psychiatric community is a plus.
This position may require significant travel due to the large geography that the incumbent will be responsible for.
Must work within 50 miles of the region?s border.
Novartis is committed to embracing and leveraging diverse backgrounds, cultures and talents to achieve competitive ad-vantage. Novartis is an equal opportunity employer M/F/D/V |
| Novartis Oncology |
na |
OR |
11/20/2009
|
| Psychiatry Sales Specialist - Eugene, OR FW2H2D |
| Bachelors degree (preferably in Life Sciences, Pharmacy or Business related discipline).
Minimum two years of pharmaceutical specialty sales experience.
At least one year of pharmaceutical sales experience in the institutional sector, preferably with Psychiatrists.
Familiarity with the Psychiatric community is a plus.
This position may require significant travel due to the large geography that the incumbent will be responsible for.
Must work within 50 miles of the region?s border.
Novartis is committed to embracing and leveraging diverse backgrounds, cultures and talents to achieve competitive ad-vantage. Novartis is an equal opportunity employer M/F/D/V |
| Johnson & Johnson Family of Companies |
Portland |
OR |
11/19/2009
|
| Portland, OR: Clinical Sales Associate: J&J Wound Management: Biosurgicals, Unit of Ethicon, Inc |
| To be considered for this role, candidates must meet the following criteria: A minimum of a Bachelor's degree. A minimum one year of outside sales experience is required. Medical Device sales experience strongly preferred. 2-5 years combined medical device and competitive business-to-business sales experience preferred. A valid driver's license issued in one of the fifty states and a clean driving record is required. The ability to work in a hospital/operating room environment is required. Willingness to travel up to 40% depending on geography is required. To be eligible for this position, applicants must currently reside in the posted territory or be willing to relocate there at their own expense. Willingness to relocate within 12 - 18 months of employment is required. If you want to explore the many small-company environments behind the big company impact of the Johnson & Johnson Family of companies, bid on this position today! |
| Novartis Oncology |
na |
OK |
11/20/2009
|
| Psychiatry Sales Specialist - Oklahoma City, OK FW2A1B |
| Bachelors degree (preferably in Life Sciences, Pharmacy or Business related discipline).
Minimum two years of pharmaceutical specialty sales experience.
At least one year of pharmaceutical sales experience in the institutional sector, preferably with Psychiatrists.
Familiarity with the Psychiatric community is a plus.
This position may require significant travel due to the large geography that the incumbent will be responsible for.
Must work within 50 miles of the region?s border.
Novartis is committed to embracing and leveraging diverse backgrounds, cultures and talents to achieve competitive ad-vantage. Novartis is an equal opportunity employer M/F/D/V |
| Novartis Oncology |
na |
OK |
11/20/2009
|
| Psychiatry Sales Specialist - Oklahoma City, OK FW2A2B |
| Bachelors degree (preferably in Life Sciences, Pharmacy or Business related discipline).
Minimum two years of pharmaceutical specialty sales experience.
At least one year of pharmaceutical sales experience in the institutional sector, preferably with Psychiatrists.
Familiarity with the Psychiatric community is a plus.
This position may require significant travel due to the large geography that the incumbent will be responsible for.
Must work within 50 miles of the region?s border.
Novartis is committed to embracing and leveraging diverse backgrounds, cultures and talents to achieve competitive ad-vantage. Novartis is an equal opportunity employer M/F/D/V |
| Novartis Oncology |
na |
OK |
11/20/2009
|
| Key Account Manager, Swine Southwest US |
| BS/BA or equivalent
? 8-10 years of experience/understanding of livestock production preferred.
? 6 years of swine experience preferred
? Ability to interpret and communicate information from a variety of technical manuals, journals and bulletins.
? Knowledgeable practices of PC package tools, including but not limited to: word-processing (Word), Spreadsheets (Excel) and Presentations (PowerPoint), e-mail (Lotus Notes).
? Valid driver operator license.
? Must reside within the boundaries of the Territory. |
| Novartis Oncology |
na |
OH |
11/20/2009
|
| Territory Sales Manager - Dallas, TX (East Dallas) |
| Minimum Education Required:
? Bachelor's degree or equivalent
Minimum Experience Required:
? 2-4 years successful outside sales experience
Preferred Level:
? One (1) year contact lens sales/opthalmic related sales/contact fitting experience.
Must have valid drivers license and the ability to travel extensively via automobile. Some air travel also required. Must successfully complete our ""New Hire Sales Training Program"". |
| Novartis Oncology |
na |
OH |
11/20/2009
|
| Sales Representative - Toledo South, OH - 3ZAE4B |
| A Bachelor's Degree * Outside sales experience with documented success in business-to-business sales preferred. * Professional accomplishments that reflect self-motivation, initiative, independence, and strong customer service orientation. In return, you'll be rewarded with: * An outstanding benefits package that includes a 401(K) and vision plan * An excellent salary and incentive awards program * A company automobile and paid expenses * Ongoing quality classroom and field training * Professional career development/growth opportunities and an educational assistance program. Novartis is an equal |
| Johnson & Johnson Family of Companies |
Cincinnati |
OH |
11/19/2009
|
| STAFF DESIGN ENGINEER - ELECTRICAL |
| BS degree in electrical engineering, or related field is required. MS degree is preferred. At least 8 years of experience in the planning, design, and commercialization of electrical or electro-mechanical systems, including embedded software is required. The ideal candidate will have a demonstrated track record of driving technically appropriate solutions and the effective use of new technology. DFSS or similar certifications preferred. Medical products or other highly regulated industry is an asset. Technical leadership and project management, particularly with globally outsourced projects is an asset. RF Analog products with experience in design, test and interconnecting/cabling is a requirement for this role. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Cincinnati |
OH |
11/19/2009
|
| Quality Systems and Compliance Specialist |
| Minimum of a BS or BA in Business, applied Sciences, Quality or an Engineering-related discipline or equivalent work experience is required. CQA certification is strongly preferred. CQE and/or CRE Certification is also preferred. A minimum of 7+ years of total work experience in Regulatory Affairs and/or Quality Assurance in a medical device or pharmaceutical environment is required. Strong auditing skills are required. Experience managing or participating in internal audit programs is also required. Strong Project Management skills, excellent verbal and written communication skills, influencing management skills are required. Knowledge of ISO-GMPs is required. Knowledge of GLP, GCP Quality Systems and international requirements is preferred. Knowledge of design and development, labeling and manufacturing systems is required. Knowledge of continuous improvement principles is preferred. Experience and/or interactions with a Regulatory agency is preferred. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! Johnson & Johnson is committed to diversity and invites all interested candidates to apply for positions of interest. EOE M/F/D/V Please note: In order to be considered eligible for an interview, candidates must apply online through the appropriate web portal. |
| Novartis Oncology |
na |
OH |
11/20/2009
|
| Territory Sales Manager - Toledo, OH |
| Minimum Education Required:
? Bachelor's degree or equivalent
Minimum Experience Required:
? 2-4 years successful outside sales experience
Preferred Level:
? One (1) year contact lens sales/opthalmic related sales/contact fitting experience.
Must have valid drivers license and the ability to travel extensively via automobile. Some air travel also required. Must successfully complete our ""New Hire Sales Training Program"". |
| Johnson & Johnson Family of Companies |
Cincinnati |
OH |
11/19/2009
|
| Clinical Scientist (1 of 2) |
| A minimum of a Bachelors degree in a biological or closely related science is required. A Masters is preferred. At minimum of 7 years of professional experience in relevant fields of health care, academic research, devices or pharmaceutical industry is required. Experience is preferable to include experience related to the conduct of clinical studies but not required. Strong scientific background and/or work experience in medicine, biology, or a closely related field. Ability to work independently. High degree of self-motivation and direction and the ability to make decisions and accept responsibility of outcomes. Strong interpersonal and negotiating skills when dealing with colleagues and outside professional contacts. 15% domestic travel is required. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Cincinnati |
OH |
11/19/2009
|
| Principal Scientist Veterinary Surgeon - Cincinnati, OH |
| A minimum of a DVM from an AVMA (American Veterinary Medical Association) approved and accredited program is required. (Board Certification is strongly preferred but not required.) A Master's and/or PhD is preferred. Advanced training including veterinary surgical residency is also preferred. A minimum of 3 years of overall research/surgical experience is required. Veterinary surgery experience utilizing veterinary models is required. Preclinical study model design experience is required. Experience as a Study Director/Leader for product evaluations is strongly preferred. Medical Device development experience is preferred. Small animal and soft tissue experience is preferred. Experience working with cross-functional groups/teams is preferred. Leadership experience/ability is strongly preferred. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Novartis Oncology |
na |
OH |
11/20/2009
|
| Psychiatry Area Sales Manager - Columbus, OH |
| Bachelors degree (preferably in Life Sciences, Pharmacy or Business related discipline). Masters degree/MBA preferred.
Must live within 50 miles of the Area?s border.
Three or more years of pharmaceutical sales experience.
At least two years of pharmaceutical sales management experience.
Preferred Qualifications: Previous experience within the anti-psychotics class or schizophrenia disease state. Calling on psychiatrists and or institutions is a plus.
This position may require significant travel due to the large geography that the incumbent will be responsible for. |
| Johnson & Johnson Family of Companies |
Syracuse |
NY |
11/19/2009
|
| Syracuse, NY - Full Line Sales Rep - Ethicon-Endo Surgery |
| To be considered for this role, candidates must meet the following criteria: A minimum of a Bachelors Degree paired with three or more years of sales experience selling to a highly educated/high profile customer base, or internal EES experience with a proven track record of achieving sales & competency objectives as a Sales Representative. The ability to sell in an operating room, lab & hospital environment is required. A valid driver's license issued in one of the 50 States with a clean driving record is required. The ability to travel as necessary, which may include overnight and/or weekends, is required. Medical device sales experience is preferred paired with documented sales results. Individuals must live within the current geography or be willing to relocate to it. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
New York |
NY |
11/19/2009
|
| New York/New Jersey: Account Manager: Therakos, Inc. a Johnson & Johnson Medical Device Company |
| To be considered for this role, candidates must meet the following criteria: Undergraduate degree required; Life Science or Science background preferred. Three to Five years of sales experience is required. Five + years of sales experience is preferred. You will need to demonstrate a record of accomplishments. Biopharmaceutical and/or Medical capital equipment sales experience preferred. |
| Johnson & Johnson Family of Companies |
Rochester |
NY |
11/19/2009
|
| Rochester, NY/Syracuse, NY/Buffalo, NY: Territory Manager (Electrophysiology) - Biosense Webster |
| To be considered for this role, the candidates must meet the following criteria: at least a Bachelor's Degree, MBA preferred. This must be coupled with at least 3 - 5 years of medical device sales experience. Candidates must have a valid driver's license issued in one of the 50 States and a clean driving record. Ability to travel as necessary, which may include overnight and/or weekend travel is required. Candidates must have excellent written and oral communication skills. Ability to work within a commission driven position with the ability to meet and exceed sales goals is required. Preference will be given to candidates with medical device sales experience in the cardiology/cardiovascular medical device industry, preferably with EP experience. Candidates with documented sales awards and achievements are also preferred. Prior Management Development classes are a plus. Preference will be given to candidates living within 30 miles of the posted geography. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Garden City |
NY |
11/19/2009
|
| Long Island, NY: Breast Care Specialist: Ethicon Endo-Surgery, Inc. |
| To be considered for this role, candidates must meet the following criteria: A minimum of a Bachelors Degree paired with three or more years of sales experience selling to a highly educated/high profile customer base. The ability to sell in an operating room, lab & hospital environment is required. A valid driver's license issued in one of the 50 States with a clean driving record is required. The ability to travel as necessary, which may include overnight and/or weekends, is required. Medical device sales experience is preferred paired with documented sales results. Individuals must live within the current geography be willing to relocate to it. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
New York |
NY |
11/19/2009
|
| Engagement Designer - Beauty |
| A Bachelor's degree is required. A minimum of 5 years of Marketing, Media, and/or Communications experience is required. Ability to create connection and experience strategies across variety of disciplines is preferred. Must understand media/communications planning, CRM, direct marketing and integrated communications. Solid qualitative and quantitative analytical skills are preferred. Ability to create communication plans that deliver maximum value is required. Must be adept at balancing brands, agencies, and connection partners to increase number of connection points, to infuse customer and brand insights, and to optimize experience, design, engagement, and success measures. Must be well versed in all touch-points and able to identify required experts to oversee experiences for actionable initiatives. Experience working with research and developing differentiating insights and actions is preferred. Experience working with media companies sales and marketing department is required. Experience working with content creation, branded entertainment, and/or new video delivery models is preferred. Experience managing high level of detail in many disciplines is preferred. Must be a strong communicator, self-starter and strategic focused. |
| Johnson & Johnson Family of Companies |
White Plains |
NY |
11/19/2009
|
| Westchester, NY- Full Line Sales Rep - Ethicon-Endo Surgery |
| To be considered for this role, candidates must meet the following criteria: A minimum of a Bachelors Degree paired with three or more years of sales experience selling to a highly educated/high profile customer base, or internal EES experience with a proven track record of achieving sales & competency objectives as a Sales Representative. The ability to sell in an operating room, lab & hospital environment is required. A valid driver's license issued in one of the 50 States with a clean driving record is required. The ability to travel as necessary, which may include overnight and/or weekends, is required. Medical device sales experience is preferred paired with documented sales results. Individuals must live within the current geography or be willing to relocate to it. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Central Islip |
NY |
11/19/2009
|
| Clinical Account Specialist Long Island, NY |
| Bachelor's Degree (or equivalent), RN, PA-C, CNP is required. MBA preferred. 2 years of experience working (i.e., sales, clinical, management, etc.) in an Operating Room and/or Catheter Lab environment is required. Candidates must have a valid driver's license issued in one of the 50 States and a clean driving record. Ability to travel up to 30% is necessary, which may include overnight and/or weekend travel. Candidates must have excellent written and oral communication skills as well as the ability to excel within a results and performance driven environment with a balanced base and variable compensation package. Ability to wear protective lead in the lab is required. Experience in the cardiology/cardiovascular medical device industry, preferably with EP experience is preferred. Candidates with documented leadership awards and achievements are also preferred. Prior management development classes are a plus. Preference will be given to candidates living within 30 miles of the posted geography. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
New York |
NY |
11/19/2009
|
| New York, NY - Sales Representative: Cordis Corporation: Cardiology |
| To be considered for this role, candidates must meet the following criteria: BA/BS in a life science or business; and a minimum of 3 years of outside sales experience. Medical device sales experience paired with Cardiology sales experience strongly preferred. Valid drivers license and clean driving record is mandatory. Candidates must be able to travel overnight as needed or requested, and must possess good written and oral communication skills. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Agilent Technologies, Inc. US |
Fishkill |
NY |
11/20/2009
|
| Field Service Technical Engineer--Account Management- NJ |
| Description : As the Field Service Engineer for a high tech growth business serving the Life Sciences markets, your primary responsibilities will include: account management, as well as, providing support on analytical LC, GC and MS products for customers, on-site. This role will provide you with the opportunity to join the Life Sciences and Chemical Analysis Group (LSCA) of Agilent Technologies.
Agilent Field Service Engineers deliver technical expertise to customers based on Agilent products and services primarily in the MS area. As an individual contributor, this job will focus primarily on large account management by providing customers with high quality services to ensure customer satisfaction. Responsibilities include on-site installation, customer training, repair and troubleshooting of hardware, and provide routine preventative maintenance, qualifications, and validation services. Other responsibilities include, adherence to environmental health and safety guidelines, understanding our customers business, parts management, coordinating resources, training, organization, providing feedback to manufacturing divisions, working with sales forces, and maintaining up to date technical knowledge for assigned products. We are looking for enthusiastic individuals who want to grow with our company and become part of a dedicated group of individuals.
~cb~11/05/09 |
| Novartis Oncology |
na |
NY |
11/20/2009
|
| Territory Sales Manager - Brooklyn |
| Minimum Education Required:
? Bachelor's degree or equivalent
Minimum Experience Required:
? 2-4 years successful outside sales experience
Preferred Level:
? One (1) year contact lens sales/opthalmic related sales/contact fitting experience.
Must have valid drivers license and the ability to travel extensively via automobile. Some air travel also required. Must successfully complete our ""New Hire Sales Training Program"". |
| Novartis Oncology |
na |
NY |
11/20/2009
|
| Psychiatry Sales Specialist - Schenectady, NY FE2C2B |
| Bachelors degree (preferably in Life Sciences, Pharmacy or Business related discipline).
Minimum two years of pharmaceutical specialty sales experience.
At least one year of pharmaceutical sales experience in the institutional sector, preferably with Psychiatrists.
Familiarity with the Psychiatric community is a plus.
This position may require significant travel due to the large geography that the incumbent will be responsible for.
Must work within 50 miles of the region?s border.
Novartis is committed to embracing and leveraging diverse backgrounds, cultures and talents to achieve competitive ad-vantage. Novartis is an equal opportunity employer M/F/D/V |
| Novartis Oncology |
na |
NY |
11/20/2009
|
| Psychiatry Sales Specialist - Queens, NY FE2F2C |
| Bachelors degree (preferably in Life Sciences, Pharmacy or Business related discipline).
Minimum two years of pharmaceutical specialty sales experience.
At least one year of pharmaceutical sales experience in the institutional sector, preferably with Psychiatrists.
Familiarity with the Psychiatric community is a plus.
This position may require significant travel due to the large geography that the incumbent will be responsible for.
Must work within 50 miles of the region?s border.
Novartis is committed to embracing and leveraging diverse backgrounds, cultures and talents to achieve competitive ad-vantage. Novartis is an equal opportunity employer M/F/D/V |
| Novartis Oncology |
na |
NY |
11/20/2009
|
| Psychiatry Sales Specialist - Long Island East, NY FE2F1E |
| Bachelors degree (preferably in Life Sciences, Pharmacy or Business related discipline).
Minimum two years of pharmaceutical specialty sales experience.
At least one year of pharmaceutical sales experience in the institutional sector, preferably with Psychiatrists.
Familiarity with the Psychiatric community is a plus.
This position may require significant travel due to the large geography that the incumbent will be responsible for.
Must work within 50 miles of the region?s border.
Novartis is committed to embracing and leveraging diverse backgrounds, cultures and talents to achieve competitive ad-vantage. Novartis is an equal opportunity employer M/F/D/V |
| Novartis Oncology |
na |
NY |
11/20/2009
|
| Psychiatry Sales Specialist - Long Island East, NY FE2F2E |
| Bachelors degree (preferably in Life Sciences, Pharmacy or Business related discipline).
Minimum two years of pharmaceutical specialty sales experience.
At least one year of pharmaceutical sales experience in the institutional sector, preferably with Psychiatrists.
Familiarity with the Psychiatric community is a plus.
This position may require significant travel due to the large geography that the incumbent will be responsible for.
Must work within 50 miles of the region?s border.
Novartis is committed to embracing and leveraging diverse backgrounds, cultures and talents to achieve competitive ad-vantage. Novartis is an equal opportunity employer M/F/D/V |
| Novartis Oncology |
na |
NY |
11/20/2009
|
| Psychiatry Sales Specialist - Lower Manhattan, NY FE2E1E |
| Bachelors degree (preferably in Life Sciences, Pharmacy or Business related discipline).
Minimum two years of pharmaceutical specialty sales experience.
At least one year of pharmaceutical sales experience in the institutional sector, preferably with Psychiatrists.
Familiarity with the Psychiatric community is a plus.
This position may require significant travel due to the large geography that the incumbent will be responsible for.
Must work within 50 miles of the region?s border.
Novartis is committed to embracing and leveraging diverse backgrounds, cultures and talents to achieve competitive ad-vantage. Novartis is an equal opportunity employer M/F/D/V |
| Novartis Oncology |
na |
NY |
11/20/2009
|
| Psychiatry Sales Specialist - Lower Manhattan, NY FE2E2E |
| Bachelors degree (preferably in Life Sciences, Pharmacy or Business related discipline).
Minimum two years of pharmaceutical specialty sales experience.
At least one year of pharmaceutical sales experience in the institutional sector, preferably with Psychiatrists.
Familiarity with the Psychiatric community is a plus.
This position may require significant travel due to the large geography that the incumbent will be responsible for.
Must work within 50 miles of the region?s border.
Novartis is committed to embracing and leveraging diverse backgrounds, cultures and talents to achieve competitive ad-vantage. Novartis is an equal opportunity employer M/F/D/V |
| Novartis Oncology |
na |
NY |
11/20/2009
|
| Psychiatry Sales Specialist - Manhattan North, NY FE2E2C |
| Bachelors degree (preferably in Life Sciences, Pharmacy or Business related discipline).
Minimum two years of pharmaceutical specialty sales experience.
At least one year of pharmaceutical sales experience in the institutional sector, preferably with Psychiatrists.
Familiarity with the Psychiatric community is a plus.
This position may require significant travel due to the large geography that the incumbent will be responsible for.
Must work within 50 miles of the region?s border.
Novartis is committed to embracing and leveraging diverse backgrounds, cultures and talents to achieve competitive ad-vantage. Novartis is an equal opportunity employer M/F/D/V |
| Novartis Oncology |
na |
NY |
11/20/2009
|
| Psychiatry Sales Specialist - Brooklyn East, NY FE2F2B |
| Bachelors degree (preferably in Life Sciences, Pharmacy or Business related discipline).
Minimum two years of pharmaceutical specialty sales experience.
At least one year of pharmaceutical sales experience in the institutional sector, preferably with Psychiatrists.
Familiarity with the Psychiatric community is a plus.
This position may require significant travel due to the large geography that the incumbent will be responsible for.
Must work within 50 miles of the region?s border.
Novartis is committed to embracing and leveraging diverse backgrounds, cultures and talents to achieve competitive ad-vantage. Novartis is an equal opportunity employer M/F/D/V |
| Novartis Oncology |
na |
NY |
11/20/2009
|
| Psychiatry Sales Specialist - Brooklyn West, NY FE2F2A |
| Bachelors degree (preferably in Life Sciences, Pharmacy or Business related discipline).
Minimum two years of pharmaceutical specialty sales experience.
At least one year of pharmaceutical sales experience in the institutional sector, preferably with Psychiatrists.
Familiarity with the Psychiatric community is a plus.
This position may require significant travel due to the large geography that the incumbent will be responsible for.
Must work within 50 miles of the region?s border.
Novartis is committed to embracing and leveraging diverse backgrounds, cultures and talents to achieve competitive ad-vantage. Novartis is an equal opportunity employer M/F/D/V |
| Novartis Oncology |
na |
NY |
11/20/2009
|
| Psychiatry Sales Specialist - Bronx, NY FE2E2B |
| Bachelors degree (preferably in Life Sciences, Pharmacy or Business related discipline).
Minimum two years of pharmaceutical specialty sales experience.
At least one year of pharmaceutical sales experience in the institutional sector, preferably with Psychiatrists.
Familiarity with the Psychiatric community is a plus.
This position may require significant travel due to the large geography that the incumbent will be responsible for.
Must work within 50 miles of the region?s border.
Novartis is committed to embracing and leveraging diverse backgrounds, cultures and talents to achieve competitive ad-vantage. Novartis is an equal opportunity employer M/F/D/V |
| Novartis Oncology |
na |
NY |
11/20/2009
|
| Psychiatry Sales Specialist - Brooklyn East, NY FE2F1B |
| Bachelors degree (preferably in Life Sciences, Pharmacy or Business related discipline).
Minimum two years of pharmaceutical specialty sales experience.
At least one year of pharmaceutical sales experience in the institutional sector, preferably with Psychiatrists.
Familiarity with the Psychiatric community is a plus.
This position may require significant travel due to the large geography that the incumbent will be responsible for.
Must work within 50 miles of the region?s border.
Novartis is committed to embracing and leveraging diverse backgrounds, cultures and talents to achieve competitive ad-vantage. Novartis is an equal opportunity employer M/F/D/V |
| Novartis Oncology |
na |
NY |
11/20/2009
|
| Multi-Skilled Craftworker II |
| ? Previous experience in Pharmaceutical, Packaging, or Manufacturing preferred.
? Minimum 5 years experience troubleshooting equipment malfunctions on electronic, pneumatic, and mechanical systems related to a manufacturing and packaging equipment.
? Experience supporting PLCs, HMIs/SCADAs, printing technologies (laser, inkjet, etc) vision/barcode systems, sensors, computer systems, industrial networks and motors (AC/DC drives, servo systems).
? The ideal candidate must be comfortable in an environment where he/she will be asked to troubleshoot equipment that is foreign to them.
? Comfortable working with and supporting computer based systems.
? Experience with continuous improvement environment (ie Lean, six sigma) a plus.
? Problem solving/critical thinking skills are required for detecting, analyzing, and resolving production problems
? Good interpersonal skills and communication skills are essential.
? Preferred: Two year degree in Automation or Electrical technology or equivalent engineering discipline.
? Certified Mechanic/Technician, Journeyman or an accredited training program certificate or equivalent. |
| AstraZeneca Pharmaceuticals |
New York City |
NY |
11/19/2009
|
| Regional Sales Specialist |
Requirements:
- A bachelor?s degree (upon hire)
- Valid drivers license and a safe driving record.
Preferred:
- Cumulative GPA of 3.0 or higher
- Previous leadership experience
- Strong communication, presentation, and project management skills
 |
| Novartis Oncology |
na |
NY |
11/20/2009
|
| District Sales Manager- New Jersey/New York City |
| Minimum Requirements:
-Four or more years of Sales Management experience in consumer products and or life sciences industries.
-6 or more years front line sales experience in consumer products and or life sciences industries.
-Experience with consultative selling.
-Bachelors degree in Business or related field.
-Strong analytic skills and experience analyzing regions and territories to discover market trend and new opportunities.
-Strong Excel and PowerPoint Skills
-Skills with Customer Relationship Management and Sales Reporting systems.
Required Skills and Experiences:
-Successful candidates will have led regions that have received top sales awards; President?s Club, Circle of Excellence, etc. and consistently be ranked in the top 10% of the selling organization.
-Demonstrated leadership as evidenced by consistently improving sales performance through people development.
-Expert knowledge in the selling process and an ability to coach and develop other?s selling skills.
-Demonstrated success selling product features and benefits rather than selling on price.
-Experience as a District or Regional Sales Manager with 7-10 direct reports.
-Strong customer orientation demonstrated through selling experiences.
-Selling and management experience in business-to-business, pharmaceutical, medical device, and or consumer products. |
| Novartis Oncology |
na |
NY |
11/20/2009
|
| District Manager I - 1ZDE - New York City |
| Bachelor's degree (preferably in Life Sciences, Pharmacy, or Business related discipline) 3 or more years of pharmaceutical sales experience At least two years of pharmaceutical sales management experience Preferred Requirements: Demonstrated ability to increase sales through facilitating relationships between managed care institutions Demonstrated ability to lead and inspire a group towards meeting and exceeding objectives Strong leadership, planning and organization, and problem solving and decision making skills. Novartis is committed to embracing and leveraging diverse backgrounds, cultures and talents to achieve competitive advantage. Novartis is an equal opportunity employer M/F/D/V. |
| Biogen Idec, Inc. |
Bronx / Upper Manhattan |
NY |
11/20/2009
|
| Area Business Manager, Neurology - Bronx / Upper Manhattan |
| Minimum 5+ years pharmaceutical sales or biotech sales experience required. Experience with reimbursement issues, product launch, and injectable/infusion product selling experience desired. |
| sanofi pasteur |
Astoria |
NY |
11/19/2009
|
| Vaccine Sales Representative - Astoria, NY |
| BA./B.S. in Immunology, Biology, Business or related field required.
2 years business to business sales or equivalent experience.
Strong oral, written and analytical skills with the demonstrated ability to work in teams.
Strong time management skills
Certifications
Driver's license is required along with a record of safe driving |
| Johnson & Johnson Family of Companies |
Rochester |
NY |
11/19/2009
|
| Program Manager |
| A minimum of a BS or higher degree in Biochemistry, Chemistry, Bioengineering or related field is required. Five years or more years of relevant technical experience with two or more years in a cross functional leadership role. Cross-functional technical or project leadership experience utilizing a phase-gate process to deliver new products into a regulated industry is required. Knowledge of project management tools and processes including facility with Microsoft Project is an asset. Experience with product project portfolio management is an asset. Design for Six Sigma experience is an asset. Experience in medical diagnostics or device industry is an asset. Experience with technical leadership of assay/reagent development is preferred and knowledge of Quality System Regulation, ISO, FDA and other regulatory requirements for medical device or diagnostic products is strongly preferred. Project Management Professional certification and/or MBA degree would be an asset. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
New York |
NY |
11/19/2009
|
| Eastern US: Key Account Manager: Therakos, Inc. a Johnson & Johnson Medical Device Company |
| To be considered for this role, candidates must meet the following criteria: Undergraduate degree required; MBA or PharmD preferred. Three to Five years of diagnostic, bio-pharmaceutical / healthcare business sales experience is required. Seven + years of sales experience is preferred. Management experience preferred. You will need to demonstrate a record of accomplishments. Biopharmaceutical and/or Medical capital equipment sales experience preferred. Candidates must live near a major airport. Ability and willingness to travel 70%, or as needed is required. |
| Johnson & Johnson Family of Companies |
Rochester |
NY |
11/19/2009
|
| ENGINEER II |
| A minimum of a Bachelors degree in Engineering or an equivalent scientific discipline is required. A minimum of 2+ years of related engineering experience is required. An Advanced degree in a relevant discipline and 3+ years of related engineering experience is preferred. Basic understanding of engineering fundamentals is required. Experience in a highly regulated industry is required. Experience in the medical device or pharmaceutical industry is an asset. Knowledge of FDA, cGMP is an asset. Knowledge of PLC, vision (camera), SCADA and HMI systems is required. Experience in manufacturing and quality systems or related applications (OTIS, QERTS, SAP) is strongly preferred. Experience with Six Sigma/Process Excellence Tools, Training, and/or Certification is preferred. Proficiency with Microsoft Project is preferred. Excellent verbal and written communication skills are required. Strong analytical/problem solving skills are a must. The ability to work on cross functional teams is required. This position will be based in Rochester, NY in manufacturing operations. |
| Johnson & Johnson Family of Companies |
Albany |
NY |
11/19/2009
|
| Albany, NY - Full Line Sales Rep - Ethicon-Endo Surgery |
| To be considered for this role, candidates must meet the following criteria: A minimum of a Bachelors Degree paired with three or more years of sales experience selling to a highly educated/high profile customer base, or internal EES experience with a proven track record of achieving sales & competency objectives as a Sales Representative. The ability to sell in an operating room, lab & hospital environment is required. A valid driver's license issued in one of the 50 States with a clean driving record is required. The ability to travel as necessary, which may include overnight and/or weekends, is required. Medical device sales experience is preferred paired with documented sales results. Individuals must live within the current geography or be willing to relocate to it. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| sanofi pasteur |
Buffalo |
NY |
11/19/2009
|
| Vaccine Sales Representative - Buffalo, NY |
| BA./B.S. in Immunology, Biology, Business or related field required.
2 years business to business sales or equivalent experience.
Strong oral, written and analytical skills with the demonstrated ability to work in teams.
Strong time management skills
Certifications
Driver's license is required along with a record of safe driving |
| Johnson & Johnson Family of Companies |
Garden City |
NY |
11/19/2009
|
| Long Island, NY: Account Manager - Ortho-Clinical Diagnostic |
| At Johnson & Johnson we are responsible to our employees, the men and women who work with us throughout the world. Everyone must be considered as an individual. We must respect their dignity and recognize their merit. To be considered for this role, candidates must meet the following criteria: A minimum if a Bachelor's degree. A BA/BS in business or health science is preferred. A minimum of 2 years of outside business to business sales experience is preferred. Valid drivers license and clean driving record is required. Ability to travel as necessary or required, which may include overnight and/or weekend travel. Excellent written and oral communication skills is required. Prior capital equipment sales experience is a plus. If you want to explore the many small-company environments behind the big-company inpact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Buffalo |
NY |
11/19/2009
|
| Buffalo/Rochester, NY: Sales Representative: Women's Health & Urology, Unit of ETHICON, Inc. |
| A minimum of a Bachelor's degree is required. A minimum of two years of outside selling experience is also required. Excellent written and oral communication skills are essential. Candidates must have a valid driver's license issued in one of the 50 United States and a clean driving record. The ability to travel as necessary (potentially overnight and/or weekend) is required. The ability to work in a lab or an operating room environment is also required. It is preferred that candidates have documented successful sales performance (ie. high growth, results vs. plan). The ideal candidate will be a self-starter with strong time management and planning skills, have the ability to target accounts and achieve results through a daily action plan, and be able to collaborate with other J&J associates (peers, marketing, Strategic Account Managers, etc.), external companies, and key opinion leaders. Medical device sales experience, in an operating room environment, is preferred, but not required. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
New York |
NY |
11/19/2009
|
| New York, NY: Clinical Sales Representative: Ethicon Products, Unit of Ethicon Inc. |
| To be considered for this role, candidates must meet the following criteria: A minimum of a Bachelor's degree, at least two years of outside selling experience, excellent written and oral communication skills, a valid driver's license and clean driving record, the ability to travel as necessary (potentially overnight and/or weekend) is required. The ability to work in a lab or an operating room environment is also required. It is preferred that candidates have documented successful sales performance (high growth, results vs. plan). Be a self-starter with strong time management and planning skills, have the ability to target accounts and achieve results through a daily action plan, and be able to collaborate with other J&J associates (peers, marketing, Strategic Account Managers), external companies (distributors) and KOL's. Operating room medical device sales experience is preferred but not required. If you want to explore the many small-company environments behind the big company impact of the Johnson & Johnson Family of companies, bid on this position today |
| Johnson & Johnson Family of Companies |
New York |
NY |
11/19/2009
|
| New York, NY:- Professional Sales Specialist - LifeScan, Inc. |
| This position requires a 4 year degree, as well as, a minimum of 2 years of outside sales experience preferred. 3-5 years of sales experience in a healthcare professional sales environment or experience in professional diabetes care or related healthcare fields strongly preferred. Candidates must have a valid driver's license issued in one of the 50 United States and a clean driving record. This position may require overnight and/or weekend travel. Excellent written and oral communication skills are essential. Preference will be given to candidates living within 30 miles of the territory, with documented history of proven sales success in outside sales, pharmaceutical, or medical products industry. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Novartis Oncology |
na |
NV |
11/20/2009
|
| Psychiatry Sales Specialist - Las Vegas, NV FW2D1A |
| Bachelors degree (preferably in Life Sciences, Pharmacy or Business related discipline).
Minimum two years of pharmaceutical specialty sales experience.
At least one year of pharmaceutical sales experience in the institutional sector, preferably with Psychiatrists.
Familiarity with the Psychiatric community is a plus.
This position may require significant travel due to the large geography that the incumbent will be responsible for.
Must work within 50 miles of the region?s border.
Novartis is committed to embracing and leveraging diverse backgrounds, cultures and talents to achieve competitive ad-vantage. Novartis is an equal opportunity employer M/F/D/V |
| Novartis Oncology |
na |
NV |
11/20/2009
|
| Psychiatry Sales Specialist - Las Vegas, NV FW2D2A |
| Bachelors degree (preferably in Life Sciences, Pharmacy or Business related discipline).
Minimum two years of pharmaceutical specialty sales experience.
At least one year of pharmaceutical sales experience in the institutional sector, preferably with Psychiatrists.
Familiarity with the Psychiatric community is a plus.
This position may require significant travel due to the large geography that the incumbent will be responsible for.
Must work within 50 miles of the region?s border.
Novartis is committed to embracing and leveraging diverse backgrounds, cultures and talents to achieve competitive ad-vantage. Novartis is an equal opportunity employer M/F/D/V |
| Novartis Oncology |
na |
NV |
11/20/2009
|
| Psychiatry Area Sales Manager - Los Angeles, CA |
| Bachelors degree (preferably in Life Sciences, Pharmacy or Business related discipline). Masters degree/MBA preferred.
Must live within 50 miles of the Area?s border.
Three or more years of pharmaceutical sales experience.
At least two years of pharmaceutical sales management experience.
Preferred Qualifications: Previous experience within the anti-psychotics class or schizophrenia disease state. Calling on psychiatrists and or institutions is a plus.
This position may require significant travel due to the large geography that the incumbent will be responsible for. |
| Johnson & Johnson Family of Companies |
Las Vegas |
NV |
11/19/2009
|
| Lab Specialist Northern Arizona (Flagstaff, AZ or Las Vegas, NV locations) |
| A minimum of a Bachelor's degree with concentration in Medical Technology or similar science concentration is required. A minimum of two years of experience as a Medical Technologist or related experience is required. Advanced Technical Certification or experience is also desired. Previous Blood Banking experience is preferred. Experience working with or training individuals on laboratory equipment. A Valid US Driver's License is required. Experience as a Chemistry/Blood Bank Supervisor or Laboratory Manager and/or Specialist is desired. Approximately 75% travel will be required for this position. A minimum of a Bachelor's degree with concentration in Medical Technology or similar science concentration is required. A minimum of two years of experience as a Medical Technologist or related experience is required. Advanced Technical Certification or experience is also desired. Previous Blood Banking experience is preferred. Experience working with or training individuals on laboratory equipment. A Valid US Driver's License is required. Experience as a Chemistry/Blood Bank Supervisor or Laboratory Manager and/or Specialist is desired. Approximately 75% travel will be required for this position.This position will be based in the Northern Arizona area (Flagstaff, AZ or Las Vegas, NV locations). If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! . If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
Albuquerque |
NM |
11/19/2009
|
| Spring Semester Co-op, Ethicon Endo Surgery (ABQ) |
| In order to be eligible for a 2010 Fall R&D Co-op position, candidate must be enrolled in an accredited college/institution and be in good academic standing pursuing a Bachelors or Masters degree in Mechanical Engineering, Biomedical Engineering or related field. Only students in their Sophomore year or above will be considered. A minimum GPA of 3.0 is strongly preferred, with demonstrated leadership/participation in campus programs and/or community service activities. Students must be available to work during session indicated and must be authorized to work in the United States and not require sponsorship in the future. To learn more about Ethicon Endo-Surgery, please visit our website at www.ethiconendo.com. |
| Novartis Oncology |
na |
NM |
11/20/2009
|
| Psychiatry Sales Specialist - Denver North, CO FC2H2C |
| Bachelors degree (preferably in Life Sciences, Pharmacy or Business related discipline).
Minimum two years of pharmaceutical specialty sales experience.
At least one year of pharmaceutical sales experience in the institutional sector, preferably with Psychiatrists.
Familiarity with the Psychiatric community is a plus.
This position may require significant travel due to the large geography that the incumbent will be responsible for.
Must work within 50 miles of the region?s border.
Novartis is committed to embracing and leveraging diverse backgrounds, cultures and talents to achieve competitive ad-vantage. Novartis is an equal opportunity employer M/F/D/V. |
| Novartis Oncology |
na |
NM |
11/20/2009
|
| Psychiatry Sales Specialist - Albuquerque, NM FC2H2A |
| Bachelors degree (preferably in Life Sciences, Pharmacy or Business related discipline).
Minimum two years of pharmaceutical specialty sales experience.
At least one year of pharmaceutical sales experience in the institutional sector, preferably with Psychiatrists.
Familiarity with the Psychiatric community is a plus.
This position may require significant travel due to the large geography that the incumbent will be responsible for.
Must work within 50 miles of the region?s border.
Novartis is committed to embracing and leveraging diverse backgrounds, cultures and talents to achieve competitive ad-vantage. Novartis is an equal opportunity employer M/F/D/V. |
| Johnson & Johnson Family of Companies |
Piscataway |
NJ |
11/19/2009
|
| MANAGER ACUTE CARE CHARGEBACKS |
| A minimum of a Bachelor's degree is required. An MBA is preferred. A minimum of 6 years business experience is required. Strong leadership skills and experience managing people directly or managing cross-functional project teams indirectly is required. Pharmaceutical Chargebacks experience or related experience is required. Knowledge of the contracting continuum is highly preferred. Strong accounting and financial skills are required. Audit skills and experience with developing, implementing and monitoring internal controls is highly preferred. Experience with Sarbanes Oxley, System Implementations and Health Care Compliance is highly desirable. This position will be based in Piscataway and will require up to 15% travel is required. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
|
NJ |
11/19/2009
|
| SAP Senior Financial Analyst (Skillman, NJ) |
| A minimum of a bachelors degree is required; a concentration in information technology, accounting and / or finance is strongly preferred. A minimum of 5 years of finance/accounting experience is required. A minimum of 5 years of SAP FICO functional experience is required. A MBA/MA/MS in business administration, MIS, accounting or finance is strongly preferred. Experience in the pharmaceutical, medical device or consumer products industries is preferred. Able to identify and diagnose SAP issues/opportunities and develop solution options is required. Able to generate complete and accurate financial postings is required. Candidate must possess excellent analytical (MS Excel), conceptual, communication and interpersonal skills. The ability to think creatively and work in a team environment is required. Individual must work well in a dynamic environment and be able to recommend and implement process improvements, work independently and handle multiple tasks simultaneously. The ability to effectively take on leadership roles in various functions is required. Individual must be able and willing to travel 10 - 15% of the time and be prepared to support financial closing cycles as required. |
| Johnson & Johnson Family of Companies |
Raritan |
NJ |
11/19/2009
|
| DIRECTOR OF MEDICAL AFFAIRS |
| Minimum of an MD or MD/Ph.D is required. At least 10 years industry experience with a proven track record in a medical/clinical environment, particularly within medical affairs in pharmaceutical industry and a specialty in Oncology is required. The individual must have have at least 4 years of experience in Oncology. Experience working within FDA requirements and other government and industry standards (HCC, etc) is required. Must have a communication style and reputation which inspires confidence by our thought leader colleagues and external professional groups. A strong record of accomplisment and peer recognition in previous leadership positions. Must possess a sound ability to act as a medical spokesperson for external audiences and strong experience developing and managing strategic relationships with medical experts and opinion leaders. This individual must possess excellent oral and written communication skills, and an effective manager of people. This role requires a deep well of expertise and global success. You must be able to travel 50% domestically and internationally. |
| Johnson & Johnson Family of Companies |
Raritan |
NJ |
11/19/2009
|
| CLINICAL RESEARCH SOLUTIONS DIRECTOR |
| BA/BS degree required; MBA preferred. At least 10 years business experience in the healthcare industry; specific experience in oncology or oncology diagnostics is preferred. Minimum of 8 years of professional sales & marketing experience with significant business to business pharmaceutical sales experience preferred. At least 8 years people management experience required. A successful and consistent track record of delivering business results in a competitive environment required. A proven track record of successful leadership and strong interpersonal and communication skills are required. Demonstrated ability to lead during periods of change, transition and growth. Demonstrated success in developing a world class organization with strong strategic, analytical and organizational skills with ability to "roll up your sleeves". Demonstrated success in leading the commercial input in collaboration with R&D. Must be able to interface with individuals at all levels of the organization. Approximately 50% domestic and international travel required. |
| Johnson & Johnson Family of Companies |
Somerville |
NJ |
11/19/2009
|
| Compensation Reporting Relationship Specialist (Sales Analytics) |
| BA/BS required. Advanced degree preferred. Minimum 5 years work experience required. Experience with Incentive Compensation Systems (i.e. Callidus, Centiv, Synergy, etc.) required. Experience with Compensation and Sales Reporting systems and data access methods required. Analytical and related Information Technology experience required. Experience working with Field Sales, Information Management / Information Technology, or Marketing organization preferred. Experience with Database structures (i.e. Oracle, SQLSERVER, etc.) and Interface technologies (i.e. Informatica, WebMethods, etc.) preferred. Proficiency (minimal to no training needed) in PC software (such as Excel, Word, PowerPoint, Microsoft Windows) required. Experience in query & report writing tools (i.e. TOAD (SQL), Microsoft Access, Cognos Impromptu, Informatica) and data access methods required. Experience with process improvement tools, e.g., SFE, LEAN/Six Sigma preferred. Additional required competencies critical to success include: Strong business acumen and technical skills; Strong organizational and communication skills; Results oriented, problem solving/resolution skills; Proactively sense and respond to problems and opportunities; Collaboration and Teaming - Ability to work in a matrix reporting structure and to be part of a project team; Internal and external customer focus; Ability to interact with senior levels of management and exercise independent judgment with regard to business decisions. This position is based in Somerville, NJ. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Sr Principal Biostatistician |
| Education Minimum/desirable): At least Masters Degree in Statistics (or equivalent degree with 6 years of experience or PhD with 2 years of experience.
Languages: Fluent English (oral or written).
Experience/Professional requirement:
1. Experience in all tasks of a Trial Statistician.
2. Proven knowledge in Statistics and its applications to clinical trials.
3. Proven knowledge of drug development and HA guidelines. Background medical knowledge preferably in relation to the specfic therapeutic area.
4. Proven knowledge of statistical software packages.
5. Good communication and presentation skills. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Sr Principal Biostatistician |
| Education Minimum/desirable): At least Masters Degree in Statistics (or equivalent degree with 6 years of experience or PhD with 2 years of experience.
Languages: Fluent English (oral or written).
Experience/Professional requirement:
1. Experience in all tasks of a Trial Statistician.
2. Proven knowledge in Statistics and its applications to clinical trials.
3. Proven knowledge of drug development and HA guidelines. Background medical knowledge preferably in relation to the specfic therapeutic area.
4. Proven knowledge of statistical software packages.
5. Good communication and presentation skills.
6. Good team player. |
| CommonHealth |
Parsippany |
NJ |
11/20/2009
|
| Medical Strategist |
| Knowledge and Skills
MD
Ideally internal medicine background with broad range of experience, especially in oncology and neuropsychiatry
Ideally, agency, med-ed and/or pharma industry experience
CommonHealth is an equal opportunity employer
|
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Onco Dir Clinical Rsch Phys |
| ? MD or PhD in Clinical Parmacology, Biochemistry or related field
? Substantial postgraduate bedside or clinical pharmacology experience in a relevant cancer treating discipline and institution required.
? Substantial experience with determining, administering, and evaluating the outcome of systemic combined modality cancer or adult hematologic malignancy treatment plans required.
? ? 3 years of involvement in clinical research or drug development in an academic or industry environment spanning clinical activities in Phases I through IV.
? Medical/scientific and operational expertise in cancer molecular medicine, biologics, and or response modifiers
? Demonstrated technical knowledge and innovation in early clinical development study designs that provide relevant evidence to decision-makers.
? Versatile knowledge and understand of pre-clinical science of oncology and all aspects of translational medicine such as toxicology, pharmacology, and regulatory requirements for early phase development in at least two relevant jurisdictions |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Oncology Global Drug Development Fellow |
| Qualifications required
Medical Doctorate (MD) degree or equivalent is required.
Advanced knowledge in Oncology, Haematology, Endocrinology required. Completion of 2-4 years of post-MD training in above area required.
Fluent oral and written English. Any other language a plus.
Knowledge, Skills, and Experience desired
Involvement in patient care and demonstrated medical/scientific expertise in oncology and/or haematology
Exposure to or demonstrated interest and knowledge in pharmaceutical company research environment
Strong interpersonal, communication, and problem solving skills.
Demonstration of general understanding of drug development process including key processes involved in protocol development, clinical trial conduct, statistical analysis of trials, and regulatory environment,
Demonstration of ability to work within a team environment and across other functions
Mobility/Citizenship
Must be able to relocate to Basel, Switzerland or New Jersey, USA for a period of one year
Current residency/citizenship of an EU country is highly preferred.
Must be able to attain the appropriate work authorization for the US in a timely fashion.
For US and Switzerland, Novartis will apply on the candidate?s behalf. |
| Johnson & Johnson Family of Companies |
Somerville |
NJ |
11/19/2009
|
| Scientist, Biosurgicals R&D |
| A minimum of a Bachelors degree is required, with a Masters degree or Ph.D. in Biochemistry, Molecular Biology, Cell Biology, Immunology or a related discipline is preferred. A minimum of 1 year of related experience is required. Must have the ability to independently design and execute experimental studies, analyze and interpret study results. In-depth knowledge and development experience in hemostasis and thrombosis, and materials design for blood-contacting applications is required. Must be able to effectively document data in notebooks, in oral presentations and writing reports. Proven track record of research and multi tasking in a Research & Development environment. Familiar with IP evaluations and product development is preferred. Previous experience in technology evaluations: an understanding of general biotechnology principles are preferred. Awareness and understanding of advanced bioanalytical techniques and test method development and validation processes are preferred. If you want to explore the many small company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today. |
| Merck & Co., Inc. |
Rahway |
NJ |
11/19/2009
|
| Biometrician |
| Requires a Ph.D. degree in Statistics or Biostatistics. Requires knowledge of statistical methodology, experimental design, and medical background. Requires solid programming expertise including a working knowledge of SAS and S-plus or R. Must be familiar with the basic operation of a computer system, other database processing systems. Must have proof of legal authority to work in the United States. Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. We offer an excellent salary and an industry-ranked benefits program, including tuition reimbursement, work-life balance initiatives and developmental programs at all levels. Merck's retirement package includes a pension plan and one of the best 401(k) plans in the nation. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition BIO002481. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Our work is someone's hope. Join us.Where patients come first - Merck Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Johnson & Johnson Family of Companies |
|
NJ |
11/19/2009
|
| Global Medical Affairs Leader (Oncology/Hematology) |
| This position requires a minimum of a MD degree, with Board Certification/Board Eligibility in Oncology or Hematology. A minimum of 5 or more years of clinical research experience is required. Pharmaceutical industry is highly desirable. For this position, experience in the Medical Affairs environment is preferred. Additionally, prior experience and/or knowledge of the prostate cancer area is strongly preferred. Knowledge of oncology products, both J&J and competitors, is required. A demonstrated track record leading highly matrixed, cross-functional work teams comprised of high-level managers and executives is required. A demonstrated track record of success within Medical Affairs and/or clinical R&D required. Global mindset and direct experience in multiple markets, proven ability to partner cross culturally/regionally is preferred as well as an in-depth knowledge of study methodology, study data reviews and analysis. In this position a successful candidate should have excellent knowledge of study execution, benefit risk management and lifecycle management.. Highly innovative with the ability to drive a complex and changing environment and effectively manage and resolve issues within the TA. Proven ability to act as a medical spokesperson for external audiences is required. Also required is strong experience developing and managing strategic relationships with medical experts/opinion leaders. Strong oral, written, and presentation skills are a must. Proven business understanding. A minimum of 20-25% domestic and international travel is required. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
|
NJ |
11/19/2009
|
| Intern - Finance MBA Leadership Development Program Summer 2010 |
| Graduate student pursuing a full time Master's Degree in Finance or Accounting or MBA Minimum of 3 years of business experience.Leadership capabilities demonstrated through extracurricular activities, employment, and/or internship experiences.Must have permanent work authorization in the U.S. without requiring sponsorship. |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Product Manager, Scientific Services |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Product Manager |
| See above |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Sr Med Scient Expert |
| MD or PhD with unique knowledge for successful clinical
program development and execution, with 3-5 years of
clinical research experience required.
- Fluent English (oral and written)
- Advanced medical/scientific writing and communication
skills
? Proven ability to interpret, discuss and represent
efficacy
and safety data relating to the assigned area.
? Proven ability to work both independently or in a cross
functional team setting, including a matrix environment.
? Demonstrated ability to establish strong scientific
partnership with key investigators in assigned TA.
? Medical and/or scientific expertise within a disease area
required; Respiratory expertise preferred |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Regulatory CMC Liaison / Biologics |
| Minimum:
Relevant scientific degree in biotechnology, biochemistry and cell biology or equivalent.
Languages:
Fluent English required (oral & written).
Experience / Professional Requirements:
? Several years of experience in regulatory preferred.
? Excellent working knowledge/experience in regulatory submissions and approval processes for Biopharmaceuticals and ability to deal with complex CMC regulatory issues and requirements
? Strong background in biopharmaceutical development (e.g. cell culture, downstream processing, analytics). Biologics experience desired
? Proven track record in successfully leading/working in interdisciplinary teams, and of planning, coordinating and leading activities simultaneously on multiple projects.
? Strong interpersonal, organizational, communication, presentation, negotiation and problem solving skills. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Sales Consultant/Sr. Sales Consultant - New Brunswick, NJ - 1ZEK4A |
| A Bachelor's Degree * Outside sales experience with documented success in Long Term Care and or Account Management experience. Alzheimer selling experience preferred. * Professional accomplishments that reflect self-motivation, initiative, independence, and strong customer service orientation. In return, you'll be rewarded with: * An outstanding benefits package that includes a 401(K) and vision plan * An excellent salary and incentive awards program * A company automobile and paid expenses * Ongoing quality classroom and field training * Professional career development/growth opportunities and an educational assistance program.
Novartis is an equal opportunity employer M/F/D/V. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Sales Representative/Consultant - Morristown, NJ - 1ZEB4B |
| A Bachelor's Degree * Outside sales experience with documented success in business-to-business sales preferred. * Professional accomplishments that reflect self-motivation, initiative, independence, and strong customer service orientation. In return, you'll be rewarded with: * An outstanding benefits package that includes a 401(K) and vision plan * An excellent salary and incentive awards program * A company automobile and paid expenses * Ongoing quality classroom and field training * Professional career development/growth opportunities and an educational assistance program.
Novartis is an equal opportunity employer M/F/D/V. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Sales Representative/Consultant - Red Bank, NJ - 1ZEK1C |
| A Bachelor's Degree * Outside sales experience with documented success in business-to-business sales preferred. * Professional accomplishments that reflect self-motivation, initiative, independence, and strong customer service orientation. In return, you'll be rewarded with: * An outstanding benefits package that includes a 401(K) and vision plan * An excellent salary and incentive awards program * A company automobile and paid expenses * Ongoing quality classroom and field training * Professional career development/growth opportunities and an educational assistance program.
Novartis is an equal opportunity employer M/F/D/V. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| SAP NetWeaver Java Application Architect |
| - University degree or equivalent in Information Technology experience
- more than 6 years of IT experience out of which last 4 years in the development and design of SAP NetWeaver Java applications (SAP Enterprise Portal and Composition Environment)
- Experience in design and governance of SAP NetWeaver Java development processes and standards desired
- Active participation in at least 2 complete implementation project cycles from blue print till post go-live support as a SAP NetWeaver Java developer
- In-depth knowledge and working experience with Enterprise Portal, Composition Environment and NetWeaver Development
- Sound knowledge of the SAP NetWeaver technology platform and related products (SOA, ESR and others)
- Java background
- Knowledge of ABAP programming language advantageous
- Excellent communication skills with a strong customer focus
- Excellent analytical skills, solution and target oriented |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Scientist, NPKPD |
| M.S. degree in biological or related sciences. Research experience using animal models is mandatory. Small animal surgical experience is highly desired. Good verbal and written communication skills are essential. The knowledge of radiochemistry, tissue distribution, metabolism and pharmacology is desirable. Prior work experience with PK/PD or statistical analysis and a demonstrated ability to work with modeling tools and databases (e.g. WinNonlin, GastroPlus, Watson, Spotfire, etc) is a plus. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Scientist, Pharmacokinetics |
| EDUCATION/EXPERIENCE:
Ph.D. with 1-3 years or MS with 5-8 years of experience in one or more areas biopharmaceutics, pharmacokinetics, drug metabolism, bioanalytical chemistry, biostatistics, PK modeling, in vivo-in vitro correlation (IVIVC), and clinical endpoint BE study design/conduct. Inhalation experience a plus. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| SDC Compliance Associate - Quality R&D |
| BS/MS in a science field with 8-10 years experience in the pharmaceutical industry.
o Good knowledge and understanding of all GMP related requirements, proficiency of regulatory and ICH guidelines
o Broad experience in the pharmaceutical industry with a strong analytical and/or manufacturing background, some R&D a plus.
o Detail oriented with Quality Assurance background with good problem solving acumen.
o Ability to work effectively in a team environment with great organization skills
o Excellent communication skills
o Critical thinking, process and performance oriented. Constant drive to improve working practices
o Provision of timely and accurate documentation to minimize submission deficiencies
o Proven performance in review of key documents by highlighting areas of deficiencies and aiding in remediation of the documentation.
o Timely follow-up and closure of Deviations, Investigations, Change Controls and CAPAs.
o Initiation of trainings and/or other appropriate measures to enhance quality and compliance within department
o Escalation of issues/alerts as appropriate to Upper Management and proposal of corrective actions |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Senior CQA Compliance Specialist |
| BA/BS or equivalent.
English (optimally a second universal language preferred).
5+ years clinical/industry/health authority experience with at least 2 years GCP auditing experience.
30-40% travel.
Ability to manage and objectively evaluate compliance issues.
Ability to maintain a moderate degree of independence with respect to decision making and problem solving.
Excellent verbal and written communication skills, team player, interpersonal skills.
Excellent computer skills, including Excel, Word, etc.
Thorough knowledge of the clinical development, clinical research processes and drug registration process/requirements required.
Thorough knowledge of GCP regulations and guidelines as well as in applicable Novartis SOPs/NIPs and Business Practices.
Good knowledge of computer validation and Part 11 requirements.
Previous experience identifying training needs, developing and conducting training programs.
Ability to multi-task and function independently as required.
Ability to operate successfully in various team capacities, including leader and/or active member.
Ability to operate successfully in various cultural environments.
Ability to coach and mentor.
Auditor certification a plus. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Senior Finance roles |
| At least 10 years of broad-based financial experience acquired in companies with rigorous and very efficient financial systems |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Senior Pathologist |
| DVM/MD degree (or equivalent) with graduate training in pathology plus 10 years experience in toxicologic pathology, or PhD in veterinary pathology plus 5 years experience in toxicologic pathology. Ability to interpret toxicologic pathology results and write reports and scientific manuscripts. Ability to supervise other personnel, when necessary. Board certification in related fields is preferred (e.g., ACVP, DABT). |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Senior R&D roles- Category Leads |
| 10-15 years of Pharmaceutical industry experience and/or Over the Counter experience in NRT
? Extensive working knowledge in development along with experience in one or more R&D functional areas (clinical, regulatory)
? Demonstrated track record of leading a complex (e.g. cross-functional, matrix designed) project team
? Demonstrated use of communication and change management strategies/tactics to influence new ways of thinking and working
? Track record of selecting, coaching and developing talent in the organization
? Successfully working across boundaries and building strong external relationships
? Success in situations requiring rigorous, analytical problem solving and the ability to determine scientific opportunity and commercial targets
? Success in effectively communicating and influencing decisions with senior management
? Understanding of global regulatory requirements and impact of public relations
? Mastery of team leadership necessary to work collaboratively with diverse parts of the business, such as marketing
? Demonstrated understanding of the interdependencies of scientific results and commercial possibilities and the use of this knowledge to make appropriate business decisions
? Awareness of cultural differences in different geographic areas and in potentially different approaches to development by an external partner
Education : Phd, Life Sciences or Medical Degree (MD) preferred |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Senior Roles-Clinical Development & Medical Affairs, R&D |
| ? MD degree
? 10+ years experience in the Pharmaceutical industry in OTC and/or Rx Clinical research with commercial savvy
? Experience with development of overall clinical strategy and development plans
? Proven management experience at a senior level
? Demonstrates leadership behaviours by providing vision and direction
? Proven knowledge of drug development processes
? Be able to effectively liaise and influence internally and externally
? Excellent communication and interpersonal skills
? Fluency in written and spoken English, knowledge of French or other European languages beneficial but not essential |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Senior Roles-Global Drug Safety & Pharmacovigilance -R&D |
| Education : MD required
Experience: ? Minimum 10 years experience in health care or pharmaceutical industry
? Minimum 4 years of experience in Drug Safety
? Minimum 4 years management experience |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Senior Roles-Global Product Development R&D |
| M.S. in Pharmaceutics or related science; PhD preferred
Experience: ? 10 -15 years experience in similar fast-paced regulated industry, OTC industry preferred.
? Diverse and extensive understanding of new drug delivery technologies in Pharmaceutical and related fields
? Proven track record of developing and launching new and innovative products in aggressive timeframes
? Excellent leadership, communication and presentation skills
? Entrepreneurial spirit, strong sense of urgency & drive, results-oriented
? Ability to realize a vision by inspiring others,
? Strong core competency in leading diverse pharmaceutical disciplines in a Team environment toward productive outcomes.
? Able to interact effectively with the most senior levels of management both internally and externally |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Senior Roles-Regulatory Affairs, R&D |
| 10+ years extensive Regulatory Affairs experience. An academic background in biological/medical sciences (preferably MD or PhD), strong diplomatic skills for dealing with regulatory agencies ability to realize a vision by inspiring and motivating others, ability to thrive and grow in a fast-paced, intellectually challenging environment, are additional important requirements. Candidate should be fluent in English. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Senior Scientific Expert: Development Licensing & Evaluation |
| University degree (diploma, PhD or MD)
1. 8 years experience within pharmaceutical industry
2. 3 years of Project management or cross functional experience
3. Advanced level of the basic science. Bring an expert level of understanding in a functional area
4. Thought Leader for the drug dev. process; expert at aligning development program goals with business needs
5. Advance knowledge of business, competitive environment and of international business practices
6. Advanced planning and tracking skills, able to see big picture, well-organized, focused on results
7. Expert leadership skills demonstrated in GPT, in staff management role or in other organizational assignments. Expert skill to optimize contribution of team members as individuals and members of a cohesive team.
8. Strong interpersonal and communication skills for bridging between scientific and business participants, for negotiating timelines and for effective international collaboration. Strong verbal communication. Expert in written communications. Strong, critical and objective interpretation of scientific and commercial information. Expert team player |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Senior Scientist (Pharmacokinetics) |
| M.S. degree in biological or related sciences with minimal 3 years laboratory experience. Research experience using animal models is mandatory. Small animal surgical experience is highly desired. Excellent verbal and written communication skills are essential. The knowledge of radiochemistry, tissue distribution, metabolism and pharmacokinetics is desirable. Prior work experience with PK/PD analysis and a demonstrated ability to work with modeling tools and databases (e.g. WinNonlin, GastroPlus, Watson, Spotfire, etc) is a plus.
THIS REQUISITION APPROVED BY TSLT ON 1-JULY-2009 AND MOVED TO CRITICAL HIRE LIST. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| SPM/AD, Product Management - Psychiatry |
| This person should have exceptional brand marketing experience and proven success in the areas of brand life-cycle management, professional and medical marketing. Business and/or biological sciences education with concentration on marketing is preferred (MBA a plus). Sales and sales leadership experience are also preferred. Peer influence skills, solid strategic thinking skills, project management and analytical skills are essential.
Strong senior management communication skills and sales force communication skills are essential.
The applicant must possess a high level of analytical and conceptual ability in order to provide strategic focus to the brand, and demonstrate a proven track record of strong execution and results. The ideal candidate will be proficient at uncovering customer based insights and leveraging this knowledge to drive brand strategy and program development. Additional requirements include the ability to lead and manage teams and multiple vendors. 20% travel is required. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Sr Brand Manager Prevacid Innovation |
| ? Proven track record of securing results on key initiatives within a consumer packaged goods or Rx environment.
? Excellent understanding and demonstrated application of brand strategy.
? Ability to lead an organization toward superior business results.
? Outstanding interpersonal skills, with emphasis on ability to influence others in all functions and at all levels in the organization.
? Understanding of the intricacies of new product development within an OTC environment a must.
? New product development experience a must with NDA experience preferred.
? College degree required, MBA preferred, and 6-8 years CPG Brand experience.
? Well-developed oral, written, and analytical skills.
In addition, this candidate will be involved in all aspects of brand strategy across the portfolio. The successful candidate could have a number of different backgrounds including packaged goods marketing, Rx marketing, market research and brand strategy. The candidate will be an excellent motivator, comfortable with both formal and influential leadership skills. The candidate must be comfortable interacting with and influencing senior management. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Sr CTH/CTH (nonMD) |
| ? ? 6 years technical, operational and managerial experience in planning, executing, reporting and publishing clinical studies in a pharmaceutical company or contract research organisation.
? Experience in multiple clinical indications and/or TAs is preferable.
? Previous experience leading in parallel several trials; leading multidisciplinary trial teams in a complex matrix environment (including remote).
? Demonstrated ability to establish effective working relationships with key investigators.
? Thorough knowledge of Good Clinical Practice, clinical trial design, statistics, regulatory processes, and global clinical development process.
? Advanced knowledge of the assigned TA is preferred, with the demonstrated capability to interpret, discuss and represent trial or program level data.
? Previous experience in interactions with Health Authorities is preferable.
? Experience in Neuropsychiatric disease areas preferred (i.e. Schizophrenia, bipolar disorder, depression) |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Sr Data Manager |
| Education: Bachelors degree in life sciences, computer science, pharmacy, nursing or equivalent relevant degrees.
Languages: Fluent English (oral and written)
Experience/ Professional Requirements:
1) Ideally 5 or more years experience in drug development with at least 4 years in Data Management activities.
2) Project team leadership experience required.
3) Good technical and problem solving skills.
4) Thorough understanding of clinical trial methodology GCP and medical technology.
5) Ability to work independently, under pressure demonstrating initiative and flexibility.
6) Attention to detail and quality focused.
7) Good organization planning and project management skills.
8) Good interpersonal and communication skills and ability to operate effectively in an international environment.
9) Good negotiation skills.
10) Thorough understanding of physiology, pharmacology, clinical study objectives and the drug development process.
11) Ability to mentor, coach within Data Management and cross functionally and train internal and external partners. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Sr Data Manager |
| Education: Bachelors degree in life sciences, computer science, pharmacy, nursing or equivalent relevant degrees.
Languages: Fluent English (oral and written)
Experience/ Professional Requirements:
1) Ideally 5 or more years experience in drug development with at least 4 years in Data Management activities.
2) Project team leadership experience required.
3) Good technical and problem solving skills.
4) Thorough understanding of clinical trial methodology GCP and medical technology.
5) Ability to work independently, under pressure demonstrating initiative and flexibility.
6) Attention to detail and quality focused.
7) Good organization planning and project management skills.
8) Good interpersonal and communication skills and ability to operate effectively in an international environment.
9) Good negotiation skills.
10) Thorough understanding of physiology, pharmacology, clinical study objectives and the drug development process.
11) Ability to mentor, coach within Data Management and cross functionally and train internal and external partners. |
| Johnson & Johnson Family of Companies |
Morristown |
NJ |
11/19/2009
|
| Product Director - REMBRANDT (Morris Plains, NJ) |
| A minimum of a BA/BS in marketing or a related business field is required. An MBA is preferred. A minimum of three years of marketing experience is required. Marketing experience in Consumer Packaged Goods environment is required. Experience working with regulated products is preferred. Candidates must have strong analytic, strategic, organizational and communications skills. Candidates must be results oriented, have demonstrated leadership abilities, and the ability to work within a cross-functional team. Experience in the following areas is preferred: Brand/Product Marketing, Strategic Marketing, Business Development, New Product Development, Advertising/Media, Consumer Promotions, Public Relations, Market Research, Contract/Pricing Management, Reimbursement, Sales Strategy/Field Sales, and working with external Agencies. This position requires up to 20% domestic travel. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
|
NJ |
11/19/2009
|
| Director, Scientific Affairs |
| An MD degree is required. One year of Medical Affairs experience is required. Experience or interest in immunology, hematology, oncology, dermatology and gastroenterology is preferred. Apherisis experience is preferred. The qualified candidate must be scientifically and clinically oriented. The qualified candidate will be someone who has a proven track record of the following: service oriented; enjoys learning and teaching; outgoing and at ease in all situations, self-starter; entrepreneurial; team oriented. Excellent oral (including presentation skills) and written communications skills are required. The qualified candidate must be willing and able to travel up to 70% of the time- both domestic and international. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Merck & Co., Inc. |
Rahway |
NJ |
11/19/2009
|
| Staff Biochemist |
| Education:BS in Biological Sciences Required. Required experience: 1 to 3 years post-bachelors degree experience in analysis and supply of biologics (may be combination of post-graduate education and/or work-related experience.) Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition #PRO007589. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Master Data Coordinator |
| See above |
| Johnson & Johnson Family of Companies |
Piscataway |
NJ |
11/19/2009
|
| Customer Contact Center Associate (Casual Part-Time) (1 of 6 Positions) |
| A minimum of a High School Diploma is required. An Associate's Degree is preferred. A minimum of 3 years of experience a fast-paced, complex Customer Service environment (i.e. Accounts Receivable, Transportation, Call Center, Distribution and/or Collections experience) is required. A minimum of 3 years of experience in a health-related service industry is preferred. Must have excellent oral and written communication skills to share information and achieve business results in a respectful and professional manner. Ability to work in a fast paced/ high volume environment with minimal supervision is required. Must have excellent time management and organizational skills and the ability to effectively prioritize. Must have strong teamwork and problem solving skills. Experience with Call Center Management tools, Web Based Order Management Systems and/or SAP is preferred. Knowledge of Microsoft Office products (Excel, Word, Outlook, etc.) is required. Knowledge of Customer Service standards, Medical Products, and following policies, procedures and SOPs is preferred. The qualified candidate will be required to work a part-time shift between the hours of 8:30 AM and 8:00 PM, Monday to Friday totaling a 19.5 hours per week with overtime, weekends and holidays as need by business. This position may require up to 5% domestic travel. Must be willing and able to work in Piscataway, NJ. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Administrative Assistant |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Accounts Receivable Associate |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| BioPharma Market Development Manager |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Finance Manager - WWIT |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| E-Business Analyst |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Distribution Manager |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Customer Service Representative |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Customer Service Associate |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Core Team Leader- R&D Platform |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Core Team Leader- R&D Platform |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Core Team Leader |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Commercial Development Manager |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Calibration Engineer |
| See above |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Manager, GCP Compliance Quality-R&D |
| Education:
Graduate degree in sciences, MD or PhD preferred
Professional Experience:
o Expert knowledge and understanding of all GCP related requirements, proficiency of regulatory and ICH guidelines
o Broad experience in clinical development in an industrial setting
o Demonstrated managerial skills in an international setting, with experience of at least 10 years in Clinical Development/Quality Assurance/Auditing
o Ability to work effectively in a team environment with great organization skills
o Excellent communication, negotiation and leadership skills
o Innovative and critical thinking, process and performance oriented. Constant drive to improve working practice |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Manager, US Project Management Supporting Global Projects |
| Education/Experience:
BS in Science related field and 10-15 years of professional related experience or Graduate Degree and 5+ years related experience in the pharmaceutical industry (preferred experience across oral solid, injectable, ophthalmic and other dosage forms). |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Manager, US Project Management Supporting Internal R&D Projects |
| Education/Experience:
BS in Science related field and 10-15 years of professional related experience or Graduate Degree and 5+ years related experience in the pharmaceutical industry (preferred experience across oral solid, injectable, ophthalmic and other dosage forms). |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Manager, US Project Management Supporting Specialty Projects |
| Education/Experience:
BS in Science related field and 10-15 years of professional related experience or Graduate Degree and 5+ years related experience in the pharmaceutical industry (preferred experience across oral solid, injectable, ophthalmic and other dosage forms). |
| Johnson & Johnson Family of Companies |
Skillman |
NJ |
11/19/2009
|
| Associate Scientist, Cell Culture (BetaLogics), 1 of 2 |
| M.S. or B.S. with a minimum of 2 years relevant experience in scientific discipline is required. Extensive experience in cell culture is required. Experience in handling human pluripotent stem cells will be given preferential considerations. Extensive experience in basic analytic skills (e.g., real-time PCR, immunohistochemistry, flowcytometry) is required. The candidate must have strong organizational and interpersonal skills along with excellent oral and written communication capabilities. Must thrive in a team-oriented and entrepreneurial environment. Due to the nature of the cell culture, the candidate must be willing to adopt a flexible work schedule. Teamwork. Provide guidance to new or junior personnel. May serve as liaison to wider internal or external scientific community. Knowledge of GLP is an asset. |
| Johnson & Johnson Family of Companies |
Skillman |
NJ |
11/19/2009
|
| Associate Scientist, Preclinical Studies (BetaLogics) |
| M.S. or B.S. with a minimum of 2 years relevant experience in scientific discipline is required. Must show basic understanding of laboratory techniques associated with work assignments. Schedule experiments in the lab and perform research in a timely, competent manner. Able to independently solve routine problems and develop solutions. Recommend modifications to methodology and understand the impact of those modifications on the broader research area. Able to review, analyze, and interpret data, especially as requires in-depth evaluation of various factors of increasing and/or changing complexity. Prepare technical reports, summaries, written protocols, and analysis. Interact with employees inside and outside of the immediate working group in a collegial, professional manner, sharing information and expertise. Foster communication and collaborative teamwork. Provide guidance to new or junior personnel. May serve as liaison to wider internal or external scientific community. Knowledge of GLP is an asset. |
| Johnson & Johnson Family of Companies |
Skillman |
NJ |
11/19/2009
|
| Associate Scientist, Cell Culture/Microencapsulation (BetaLogics) |
| M.S. or B.S. with a minimum of 2 years of relevant experience in a scientific discipline is required. Knowledge of GLP is preferred. Extensive experience in cell culture is required. Experience in handling human pluripotent stem cells will be given preferential considerations. Extensive experience in basic analytic skills (e.g., real-time PCR, immunohistochemistry, flowcytometry) is required. The candidate must have strong organizational and interpersonal skills along with excellent oral and written communication capabilities. Must thrive in a team-oriented and entrepreneurial environment. Due to the nature of the cell culture, the candidate must be willing to adopt a flexible work schedule. Teamwork. Provide guidance to new or junior personnel. May serve as liaison to wider internal or external scientific community. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Product Director/Assc Dir Regional Marketing Leader |
| Education: University degree in marketing or related
Fluent English and Spanish preferred
7-10 years operational marketing / product management experience (including Country-level product management, fast moving consumer goods branding or marketing support functions)
Pharmaceutical sales experience (minimum 6 months sales rep rotation)
International experience or worked with international marketing teams as a local product manager
Launch experience with new products or major line extensions
Experience in clinical development or Pharma project management
Experience in pharmaceutical brand/product communications
Exposure to multi-country product launches
Bilingual in English/Spanish is strongly preferred
Therapeutic areas of expertise - Oncology, Transplant, or AIDS is stongly preferred. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Regional Associate Director US Clinical Operations, Oncology |
| ? BS degree in a scientific or health care discipline.
? Expert in Oncology with established contacts in the medical community
desired
? Demonstrated skill sets, competency, and proficiency in clinical research
and relevant people management skills.
? Thorough understanding of international aspects of the drug development
process
? Extensive knowledge of GCP/ICH, FDA, local regulations, and trial
monitoring practices
? Matrix management skills in a local and global environment
? Excellent writing, oral and interpersonal communication skills as well as
strong organizational skills
? Proficiency in relevant computer software applications
? Ability to travel a minimum of 50%
? Ability to interact/communicate in matrix organization.
? At least 6 years experience in clinical research.
? At least 2 years supervisory experience is preferred.
? At least 5 years monitoring experience is preferred.
? Experience in project management a Plus
? Strong computer knowledge in Word, PowerPoint, Excel and Lotus Notes
At least 6 years |
| Merck & Co., Inc. |
Rahway |
NJ |
11/19/2009
|
| Co-op Pilot Plant Operations |
| This position requires students to be in their Sophomore, Pre-Junior, or Junior year, pursuing a Bachelors of Science (B.S) in Chemical or Mechanical Engineering. A minimum Grade Point Average (GPA) of 3.0 is preferred. Prior pharmaceutical experience is a plus. This position is based in Rahway, NJ. Candidate must be available for a period of 6 months. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers . to create a profile and submit your resume for requisition # ADM004029. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| HR Business Strategy Leader |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Laboratory Technician |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Internal Audit Director |
| See above |
| Merck & Co., Inc. |
Whitehouse Station |
NJ |
11/19/2009
|
| MMD MS Chemistry College Recruiting |
| QualificationsThis position requires candidate to be currently enrolled in a MS program in Chemistry or Biochemistry. Ideal candidate will possess superior communication and interpersonal skills. Laboratory experience is preferred. Must be graduating between August 2009 and August 2010. Candidates must be eligible to work in the US without sponsorship. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # CHE002122. |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Sr Brand Manager, Hospital & Insitutional |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Senior Quality Engineer, Pen Injection Platform |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Senior Project Engineer - Molding |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Senior Project Engineer - Assembly |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Senior Product Manager - Vaccines |
| See above |
| Johnson & Johnson Family of Companies |
New Brunswick |
NJ |
11/19/2009
|
| Director, Pension Funds |
| A minimum of a Bachelor's degree in Finance, Business or a related discipline is required. An MBA and/or Chartered Financial Analyst (CFA) certification is required. A minimum of five years of job related experience is required. An understanding of financial markets and/or investments is required. An understanding of public and private securities is preferred. Experience in analyzing a variety of asset classes and developing investment opportunities is required. Ability to demonstrate strong investment judgment and perspective as it relates to employee benefit funds is desired. A working knowledge of statistics and computerized applications as well as databases common to the investment community is preferred. An understanding of the fiduciary duties and legal environment in which employee benefit funds exist is preferred. The ability to travel domestic and international approximately 10% is required. |
| Johnson & Johnson Family of Companies |
|
NJ |
11/19/2009
|
| R&D Co-Op- Fall 2010 |
| Candidates must be working towards a B.S., M.S., or PhD degree in Chemical Engineering, Materials (Science) Engineering, Biological or Biomedical Engineering, Biology, Chemistry, Pharmaceutical Sciences, or other related concentration. Candidates must possess a 3.0 GPA or higher. Candidates must be authorized to work in the U.S. for any employer. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Pharmacovigilance Leader (PVL MD) |
| Experience/Professional:
3 years clinical experience postdoctoral
requirement:
At least 3 years in drug development in a major pharmaceutical company including 2 years in drug safety at an operational or medical position
Proven ability to analyze, interpret, discuss, and represent safety information both in writing and orally.
Experience in preparing or contributing to preparation of clinical safety assessments and regulatory reports/submissions involving safety information.
Experience with (safety or others) issue management
Experience in drug development, clinical trial methodology, regulatory requirements, scientific methodo logy, statistics and writing of publications
Education (minimum/desirable): Medical Degree required. Specialty Board certification desirable. Useful additional degrees: Post graduate degree in Pharmaceutical Medicine; Master of Public Health in Epidemiology (or equivalent) |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Program Section Leader (PSL MD) |
| Education:
Advanced degree or equivalent education/degree in life science/healthcare is required. MD, PhD degree preferred.
Advanced knowledge in medical/scientific area required.
? ?8 years of involvement in drug development spanning clinical activities in Phases II/IV or comparable experience in industry.
? ?4 years of demonstrated leadership and accomplishment in all aspects of conducting clinical trials (e.g., planning, executing, reporting and publishing), or section of clinical programs in a global/matrix environment (including remote) in pharmaceutical industry.
? ?4 years people management experience required, this may include management in a matrix environment. Global people management experience desirable.
? Strong management, interpersonal, communication, negotiation and problem solving skills.
? Considerable organization awareness (e.g., inter-relationship of departments, business priorities), including significant experience working cross-functionally and in global teams.
? Medical/scientific and operational expertise appropriate to the program. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Program Section Leader (PSL MD) |
| Education (minimum/desirable):
Advanced degree or equivalent education/degree in life science/healthcare is required. MD, PhD degree preferred.
Advanced knowledge in medical/scientific area required.
Languages:
Fluent oral and written English.
Experience/Professional requirement:
? ?8 years of involvement in drug development spanning clinical activities in Phases II/IV or comparable experience in industry.
? ?4 years of demonstrated leadership and accomplishment in all aspects of conducting clinical trials (e.g., planning, executing, reporting and publishing), or section of clinical programs in a global/matrix environment (including remote) in pharmaceutical industry.
? ?4 years people management experience required, this may include management in a matrix environment. Global people management experience desirable.
? Strong management, interpersonal, communication, negotiation and problem solving skills.
? Considerable organization awareness (e.g., inter-relationship of departments, business priorities), including significant experience working cross-functionally and in global teams.
? Medical/scientific and operational expertise appropriate to the program. |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Manager, Corporate Communications |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Manufacturing Integrator, Diabetes Care |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Principal Engineer - Technical Lead |
| See above |
| BD (Becton, Dickinson and Company) |
Teterboro |
NJ |
11/20/2009
|
| Pilot/Aircraft Captain Corporate Flight Department |
| See above |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Principle Med Scien Expert MD |
| ?Advance medical/scientific writing and communication skills.
?Proven ability to interpret, discuss and represent efficacy and safety data relating to the assigned area.
?Proven ability to work both independently or in a cross functional team setting, including a matrix environment.
?Demonstrated ability to establish strong scientific partnership with key investigators in assigned TA.
?Medical and/or scientific expertise within a disease area nephrology/transplantation required. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Principal Scientist (GMP Facility Manager/Engineer) |
| Education
Minimum: BS/MS or equivalent with greater than 8 years of experience.
Desirable: Advanced degree in a scientific or relevant discipline (Ph.D. or equivalent) with a minimum of 5 years of experience.
Languages: Fluent English (oral and written)
Experience/Professional Requirement:
1. Successfully demonstrated several years (minimum of 3 years) of directly related experience as senior scientist of Ph.D. with post-doctoral/industrial experience (minimum of 1 year) or equivalent.
2. Successfully demonstrated expertise in a specific scientific/technical area.
3. Recognized achievements in the development of new lab/plant procedures.
4. Excellent knowledge of laboratory and/or technical tools.
5. Proficient in utilization of special tools/equipment, lab automation tools and specialized facilities e.g., containment/sterile labs.
6. Thorough understanding of development activities and processes in a specific function.
7. Good knowledge of software and computer tools.
8. Profound literature search skills.
9. Good presentation skills and scientific/technical writing skills.
10. Strong scientific leadership skills.
11. Strong knowledge of relevant SOP, GLP, GMP and Novartis regulations and policies. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Principal MSE |
| MD or PhD with unique knowledge for successful clinical program development and execution, with > 6 years of clinical research experience required.
- Fluent English (oral and written)
- Advanced medical/scientific writing and communication
skills
? Proven ability to interpret, discuss and represent efficacy
and safety data relating to the assigned area.
? Proven ability to work both independently or in a cross
functional team setting, including a matrix environment.
? Demonstrated ability to establish strong scientific
partnership with key investigators in assigned TA.
? Medical and/or scientific expertise within a disease area
required. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Postdoctoral Fellow, DMPK |
| Ph.D. degree with 0-3 years of post-PhD research experience in pharmacokinetics, biopharmaceutics, biomedical engineering, chemical engineering, or other related discipline with specific experience in PK/PD and/or PK modeling is required. The candidate must be able to work independently and have a strong understanding of PK/PD. The candidate should should be able to provide technical assistance on individual projects, spanning across multiple therapeutic areas. Hands-on experience in PK and PK/PD modeling is a must. Good oral and written communication skills are required. Previous experience with some of the PKPD softwares such as: WinNonlin; ADAPT; NONMEM, GastroPlus. |
| Johnson & Johnson Family of Companies |
New Brunswick |
NJ |
11/19/2009
|
| PAYROLL TAX ANALYST |
| Minimum of a Bachelors Degree is required, prefer a major in Finance/Accounting or Business Administration. Minimum of two years payroll or finance related experience is required.Knowledge of country payroll and tax filing requirements (for at least one of the countries this role supports) is required. Experience in the countries preferred (and several languages, as appropriate). Outsourced payroll experience preferred. This role requires the ability to influence others, identify problems and recommend course of action is required. Experience with Microsoft Office Tools is required. Experience with SAP a plus. Demonstrated ability to respond promptly, thoughtfully and effectively to changing work environments, changing priorities, and new situations and excellent organizational skills as well as oral and written communication skills are required for this role. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Dir Clinical Rsch Physician, Oncology |
| The successful candidate should have an MD and be Board Certified or board eligible in either hematology or oncology with several years (2 + years) of oncology/hematology clinical research experience in the industry.
Essential requirement will be excellent presentation skills and strong background scientific knowledge base in Hematologic malignancies.
Experience in both Clinical Development and/or Medical Affairs is preferable or a combination of experience in academic medicine with clinical research and/or 1 year of clinical development experience within the pharmaceutical industry.
Experience leading the design, conduct, analysis and reporting of oncology clinical studies is desirable.
Should have demonstrated significant successful interactions with oncology key opinion leaders/investigators.
Candidates should have demonstrated the capability for strategic planning along with operational skill and experience related to clinical research involving both single and multiple centers.
Ability to work across multiple functions is essential. Effective oral and written communication skills and strong leadership are sought. |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Medical Specialist |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Molding Technology Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Metallurgist/Materials Engineer |
| See above |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Patent Attorney II |
| EDUCATION/EXPERIENCE:
Requires significant Hatch-Waxman experience, J.D./L.L.M., B.S. or M.S., preferably Ph.D. and 5-10 years related work experience. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Patent Attorney III |
| EDUCATION/EXPERIENCE:
Requires significant Hatch-Waxman experience, J.D./L.L.M., B.S. or M.S., preferably Ph.D. and 8+ years related work experience. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Paralegal |
| Education : B.A./B.S. and/or Paralegal Certificate from ABA Certified Paralegal Studies Program
Experience: Minimum 5 years experience in all aspects of US patent prosecution including PCT. Experience with PAIR and electronic patent application filing. Experience learning different electronic data systems and synthesizing data systems together to create more efficient work processes. Strong interpersonal and teamwork skills. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Manager Business Planning |
| ? BS/BA/CPA in Finance or Accounting and MBA strongly preferred
? 3 ? 5 years of directly and progressively responsible experience and demonstrated achievement in financial analysis, with a focus on improving analytical decision making, preferably in the pharmaceutical industry
? Broad understanding of various financial management areas such as financial statement analysis, accounting, budgeting, profitability analysis, costing, consolidated financials
? Excellent knowledge of Excel and Powerpoint with working knowledge of SAP R3, BW, TM1 and Business Warehouse or other data warehousing applications desirable
? Highly motivated self-starter with a willingness to assume responsibility, take ownership for their work and intelligently challenge the status quo
? Possesses a strong sense of urgency to meet deadlines, while maintaining attention to detail and quality of work
? Strong team player than can work effectively in cross-functional teams
? Strong analytical skills with the ability to recognize problems, develop solutions and implement them
? International mindset and ability to work in a multi cultural environment
? Excellent communication skills, both verbally and in writing; ability to relay financial information to non-finance groups and interface with all levels of management |
| Teva Pharmaceuticals USA |
Fairfield |
NJ |
11/20/2009
|
| Security Officer |
|
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Operations Expert - Clinical Quality Assurance |
| Life-Science degree or equivalent. Project Management Certification.
8-10 years pharmaceutical industry experience preferred, with 5+ years in Clinical Development or Quality Assurance, with a detailed knowledge of clinical drug development process.
Audit experience strongly preferred.
Expert knowledge of international regulatory environment (GCP, at minimum US and EU regulations and ICH).
Demonstrated Project Management Training/Experience, or at least 2 years people management experience.
Demonstrated adult learning/training experience.
Ability to work globally and initiate and co-ordinate the work of associates at all levels required in managing global projects from initiation to completion.
Ability to communicate concepts and ideas verbally and in writing.
Good negotiation and interpersonal skills.
Expert planning and tracking skills.
Well organized.
Focused on results.
Capable of managing multiple projects / multi-tasking; excellent time management with respect to priorities and self management. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Onco Dir Clinical Res Phys |
| The successful candidate will be required to have Board Certification in Oncology and Hematology with a minimum of 2+ year of industry experience managing clinical research or 5+ years of relevant medical/clinical experience.
? Experience in previous management and accountability for budget execution is desirable.
? Previous experience in collaborative interactions on clinical studies with investigators globally is very important
? Previous experience managing CRO interactions related to clinical study operations is highly desirable.
? Candidates should have demonstrated the capability for strategic planning along with operational skill and experience related to clinical research involving both single and multiple centers. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Medical Safety Expert II |
| Education:
MD required
Experience:
Minimum 5 years experience in health care or pharmaceutical industry with a minimum of 2 years in Drug Safety*, Minimum 1 year OTC ex-perience, Signal detection and risk management plan experience re-quired. Management experience preferred
*Experience requirement can be reduced with advanced education or equivalent relevant clinical experience |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Medical Dir/Senior Medical Director US Medical NSO (Neuroscience) |
| A MD degree with 3-7 years? clinical trial experience and Board Certification/Eligibility in Neuroscience is required; direct pharmaceutical industry experience will be a plus.
? Experience in managing clinical trial conduct for neurological disorders is essential.
? Firm working knowledge of GCP, scientific and clinical methodology, protocol design, project management and regulatory requirements for clinical studies designated for review by regulatory authorities.
? Medical Affairs and U.S. marketing experience, to include a well documented history in medical development of neuroscience therapeutics and of bridging proactive relationships among product development, clinical development and marketing teams.
? Strategic business perspective required to bring launched and pre-launch compounds forward as commercially viable drugs.
? A well-established network within the medical research community that will attract high-caliber professionals into the Novartis organization.
? Proven ability to build productive relationships and teams internally and externally, and the ability to develop high potential subordinates into leadership roles.
? Reputation as an open, available and transparent communicator.
? Strong leadership and organizational skills; demonstrated personnel management capabilities.
? Experience leading large projects/organizations.
? Excellent oral and written communication skills. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| MBA Summer Internship - Marketing 2010 |
| 1st year MBA candidates that have experience in the areas of marketing and/or the pharmaceutical industry. Candidates should possess strong analytical, interpersonal and project management skills and should also desire to become a participant in our Commercial Development Rotational Program upon graduation to begin their career in marketing within the Pharmaceutical industry. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| MBA Summer Internship - Finance 2010 |
| 1st year MBA candidates that have experience in the areas of corporate finance (preferred). Candidates should possess strong analytical, interpersonal and project management skills and should also desire to become a participant in our Finance Leadership Development Program upon graduation to begin their career in finance within the Pharmaceutical industry. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| MBA Brand Marketing Internship 2010 |
| This opportunity is limited to first year MBA students only.
? Internship with consumer packaged goods company or prior marketing experience a plus.
? Demonstrative strategic and creative problem solving skills
? Strong analytical skills and leadership skills particularly of cross-functional teams
? Excellent oral and written skills and proactive self-starter.
? Broad understanding of brand management principles.
? Knowledge of sales and marketing principles and awareness of market research methods.
? Computer efficiency required (Word, Excel, PowerPoint, Lotus notes preferred).
? Ability to analyze and summarize marketplace dynamics. |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Principal Engineer- R&D Platform |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Principal Engineer, Mechanical Engineer - Hypodermic team |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Principal Engineer, Environmental Packaging |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Rebate Reconciliation Associate |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| VP Manufacturing Injection |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| R&D Manager, Emerging Markets |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| R&D Manager, Technology Development |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Quality Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| R&D Director, Additive and Chemistry |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| R&D Director, Preanalytical Systems |
| See above |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Brand Safety Leader(CVM MD) |
| Education (minimum/desirable): Medical degree required, Specialty Board certification desirable. Useful additional degrees: Post graduate degree in Pharmaceutical Medicine; Master of Public Health in Epidemiology (or equivalent)
Languages: Fluent in spoken and written English,
Understanding in another language (e.g. French, German, Spanish) desirable.
3 years clinical experience postdoctoral
? At least 5 years are in drug development in a major pharmaceutical company (of which 2 years in a global position), including 2 years in safety at an operational or medical position-
? Experience in preparing or contributing to preparation of clinical safety assessments and regulatory re-ports/submissions involving safety information.
? Experience in leading cross-functional, multi-cultural teams
? Experience with (safety or others) issue management
? Experience in drug development, clinical trial methodology, regulatory requirements, scientific methodology, statistics and writing of publications |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| BSL |
| ? 3 years clinical experience postdoctoral
? At least 7 years of experience in drug development in a major pharmaceutical company, or CRO, or Health Au-thority, including at least 5 years of experience in clinical safety (of which at least 3 years in a global posi-tion)
? Experience in preparing clinical safety assessments, risk/benefit evaluations and regulatory reports
? Experience in leading cross-functional teams
? Experience with safety issue management
? Experience in preparing development documents such as Safety Strategy in Clinical Development Plans, Inves-tigator Brochure
? Knowledge or degree in pharmacokinetics or pharma-cology would be of benefit |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Buyer I |
| EducationExperience:
AS/AA and 3-5 years of professional related experience. Demonstrated proficiency in SAP and Ariba Buyer. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Clinical Research Manager |
| Four-year university degree (BA/BS). Degree in Life Sciences, Nursing, or equivalent, preferred.
1. Minimum 7 - 10 years experience in drug development for this Clinical Research Manager (CRM) role.
2. Industry experience in a variety of areas with increasing levels of responsibility
3. Knowledge of clinical trial design; basic statistics and pharmacokinetics
4. Solid medical/scientific writing skills; ability to effectively communicate across the business organization, both upward and downward.
5. Knowledge of Oncology therapeutic area strongly preferred. Experience with Solid tumor studies beneficial.
6. Knowledge of good clinical practices (GCP/ICH) and regulatory requirements.
7. Basic working knowledge of clinical database systems.
8. Strong experience and knowledge of basic Microsoft Office computer programs (i.e., word, excel, and project) required. Basic knowledge and experience with Microsoft access a plus.
9. Ability to collaborate and work effectively in teams.
10. Fluency in English (oral and written) required. Conversation ability in other languages a plus.
11. Demonstrates competencies in line with established profile. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Clinical Research Scientist/Sr. CRS |
| 1. Minimum 2 years experience in drug development for CRS role. Clinical trial experience preferred.
2. Basic working knowledge of clinical database systems
3. Knowledge of clinical trial design; basic statistics and pharmacokinetics a plus.
4. Solid medical/scientific writing skills; ability to effectively communicate across the business organization
5. Knowledge of Oncology therapeutic area
6. Knowledge of good clinical practices (GCP/ICH) and regulatory requirements.
7. Ability to collaborate and work effectively in teams.
8. Demonstrates competencies in line with established profile.
9. Ability to manage multiple projects simultaneously.
10. Effectively manage project goals/objectives and timelines.
11.Collaborate with cross functional areas to support project deliverables.
12.Up to 20% travel |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Clinical Trial Budget Manager |
| Bachelor Degree required, preferred in Life Science or Business Administration. Advanced degree preferred (e.g. MBA, MPH, PhD).
1. 2-5 years of pharmaceutical industry experience, with previous experience in either clinical research or finance, in a healthcare environment.
2. Strong financial background.
3. Knowledge of clinical development processes and guidelines.
4. Experience in working with electronic databases, clinical and/or project management planning and reporting systems.
5. Proven effective communication skills.
6. Ability to work on cross-functional global teams. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Clinical Trial Head (Phase 3) |
| Impact on organization:
Responsible for financial/resource decisions within scope of assigned authority.
Well managed and effective trial team(s) resulting in the timely delivery of high quality analysis of clinical trial data which enables strategic decisions within the clinical program.
Education:
Advanced degree or equivalent education/degree in life science/healthcare is strongly recommended. MD, PhD preferred.
Minimal Requirements:
? 5+ years technical, operational and managerial experience in planning, executing, reporting and publishing clinical studies in a pharmaceutical company or contract research organisation.
? Proven ability to work independently, to lead a multidisciplinary trial team in a complex matrix environment (including remote).
? Experience in developing effective relationships with key investigators.
? Thorough knowledge of Good Clinical Practice, clinical trial design, statistics, regulatory processes, and global clinical development process.
? Advanced knowledge of the Oncology and/or Hematology is preferable. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| CMC Liaison - Pain - Global Regulatory Affairs |
| Education:
- Minimum BA, BS; Preferred MA, MS, PhD, PharmD in Life Science
- Experience:
5+ (Manager) to 8+ (Senior Manager /Associate Director) years in Regulatory Affairs
- Strong successful experience in driving international regulatory activities (Europe, rest of the world) with respect to CMC filing, variations and management of HAs requests - International exposure
- Multicultural skills - strong communicator and customer oriented |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| CTH / Sr CTH (nonMD) |
| ? ? 6 years technical, operational and managerial experience in planning, executing, reporting and publishing clinical studies in a pharmaceutical company or contract research organisation.
? Experience in multiple clinical indications and/or TAs is preferable.
? Previous experience leading in parallel several trials; leading multidisciplinary trial teams in a complex matrix environment (including remote).
? Demonstrated ability to establish effective working relationships with key investigators.
? Thorough knowledge of Good Clinical Practice, clinical trial design, statistics, regulatory processes, and global clinical development process.
? Advanced knowledge of the assigned TA is preferred, with the demonstrated capability to interpret, discuss and represent trial or program level data.
? Previous experience in interactions with Health Authorities is preferable.
? Experience in Neuropsychiatric disease areas preferred (i.e. Schizophrenia, bipolar disorder, depression) |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Demand Analyst |
| - 1-2 years of experience as analyst in a large corporation. Previous consumer products and forecasting experience a plus
- The position requires the individual to be exceptionally detail oriented and well organized
- Exposure to SAP APO forecasting module, familiarity with DRP planning systems, IRI and a Business Intelligence (BI) reporting tool
- The individual must have strong analytical, interpersonal and communication skills. Ability to handle and understand large amount of data and communicate demand to various levels of organization
- Expert in MS Excel & Access with ability to build and modify Pivot tables, Access Data bases, Reports
- Strong follow up skills
- Strong time management & multitasking skills
- Bachelors Degree required |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| R&D Manager, Packaging Technology |
| See above |
| Johnson & Johnson Family of Companies |
Somerville |
NJ |
11/19/2009
|
| 2009 Fall Co-ops - Ethicon and Closure Medical |
| Candidate must be enrolled in an accredited college/institution and be in good academic standing Student must be currently pursing a BS or Graduate Degree. Must be available to work full time (40 hours/week) during the 2009 Fall semester. |
| Johnson & Johnson Family of Companies |
Somerville |
NJ |
11/19/2009
|
| 2009 Fall R&D Co-op |
| Candidate must be enrolled in an accredited college/institution and be in good academic standing Student must be pursing a BS or Graduate Degree in Mechanical Engineering, Materials Science and Engineering, Bioengineering, Electrical or related field. Must be available to work full time (40 hours/week) during the 2009 Fall semester. This position will be located in Somerville, NJ. |
| Johnson & Johnson Family of Companies |
Somerville |
NJ |
11/19/2009
|
| Director Health Economics and Reimbursement SNS (Selective Nerve Stimulator) |
| A minimum of a Masters degree in biomedical science, health service research, business or economics is required. Post doctoral experience is also desirable. Health services research and clinical epidemiology experience preferred. At least 5 or more years experience in HE&R function in pharma, biotech, device or other relevant health care environment required. At least 2 or more years experience in device reimbursement required. Strong knowledge of the US and EMEA healthcare system. Prior experience interfacing directly with Evidence-based medicine and Research and development teams. Knowledge of the needs and expectations of regional payers, insurers and commercial customers in our strategic markets. Strong knowledge of evidence generation and value proposition strategy development used in R&D new product development process in order to provide support for price and market access. Experience in leading cross- functional teams to deliver and communicate evidence generation strategy and customer requirements. Experience with the methods and research tools used in Outcomes research, including clinical epidemiology, health economics and health series research. Ability to author, co-author, publish, referee and critique manuscripts relevant to product value. Demonstrated ability to provide constructive and innovative input into complex problems. Good judgment in business decision making. Ability to create a strategic plan by integrating short-, mid-, and long-term objectives. Ability to clearly communicate to a variety of audiences, both big picture ideas as well as technical details. A proven track record of being able to integrate their own thinking and activities into the work of other teams. Experience of developing concise and audience-focused communications, both written and for presentation. Project management experience. Ability to lead and support change. Significant accomplishments and leadership demonstrated internally; externally recognized as a credible peer/leader. Excellent communications and presentation skills; Excellent interpersonal skills. Ability to represent J&J in a leadership capacity at a variety of external forums. Customer centricity - ability and appreciation to clearly understand that customer and their unique needs; ability to translate understanding into effective development and delivery of relevant solutions. Must have skills in the following: Collaboration and teaming; Strategic Thinking; Ability to make sound business decisions; Intellectual Curiosity; ability to be results oriented. Up to 20% US-based travel is required. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Regulatory Affairs Specialist |
| See above |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Integrated Information Sciences&Operations(IIS) Global Program Head |
| Minimum: Advanced degree in science or relevant discipline or equivalent
Languages: Excellent English required (oral & written). Good skills in site (local) language desired (oral).
Experience/Professional requirement: Minimum 10+ in drug development and 5-7 years managing teams.
Demonstrated leadership and management skills. Expert skills in managing and directing global multifunctional teams to a shared vision and a common goal.
Drug Development domain expert in clinical trial methodology: planning, execution, and reporting.
Project management proficiency.
Proven track record in working across a matrix organization and demonstrates skills in building partnerships, negotiating agreements; excels at collaboration |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| HR Generalist |
| Education/Experience:
Bachelors Degree required Masters Degree in HR preferred.
1 or 2 Internships in a Human Resources generalist capacity required.
Detail orientated and excellent communication skills, strong experience with Lotus Notes, PowerPoint and Microsoft Office required.
Applicant Tracking System and Peoplesoft experience preferred. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| HR Summer Internship 2010 - Master Level |
| Bachelor's Degree with 1 year towards Masters Degree
? 3-7 years Human Resources experience
? Data management experience; Excel, Access, PowerPoint proficiency
? Strong verbal and written communication skills
? Analytical skills
? Strong project and time-management skills
? Exceptional organizational and time management skills
? Excellent follow-through and attention to detail
? Ability to work independently
? Knowledge of political environment and healthcare policy ? preferred |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| IMS Unit Head -OTM |
| ? 3 years clinical experience postdoctoral
? At least 7 years in drug development in a major pharma-ceutical company (of which 5 years in a global position), including 5 years in safety at an operational or medical po-sition
? Experience in early clinical development/translational medicine and in due diligences
? Experience in preparing of clinical safety assessments and regulatory reports/submissions involving safety informa-tion.
? Experience in leading cross-functional teams.
? Experience in drug development, clinical trial methodology, regulatory requirements, scientific methodology, statistics and writing of publications
? Desirable: Management experience |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Global Program Medical Director |
| ? MD required. Advanced knowledge in medical/scientific area required.
Languages:
Fluent oral and written English
Experience/Professional requirement:
? ? 10 years of involvement in drug development spanning clinical activities in Phases II/IV or comparable experience in industry.
? ? 5 years of demonstrated leadership and accomplishment in all aspects of conducting clinical trials (e.g., planning, executing, reporting and publishing), or section of clinical programs in a global/matrix environment (including remote) in pharmaceutical industry.
? ? 5 years people management experience required, this may include management in a matrix environment. Global people management experience desirable.
? Strong management, interpersonal, communication, negotiation and problem solving skills.
? Considerable organizational awareness (e.g., inter-relationship of departments, business priorities), including significant experience working cross-functionally and in global teams.
? Medical/scientific and operational expertise appropriate to the program.
? Demonstrated technical knowledge and innovation in clinical development study designs that provide relevant evidence to decision-makers.
? Prior history with post-marketing/brand optimization studies to obtain evidence of brand value and support commercialization activities preferred. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Global Program Medical Director |
| Education (minimum/desirable):
? MD required. Advanced knowledge in medical/scientific area required - focus is on the Cardiovascular therapeutic area.
Languages:
Fluent oral and written English
Experience/Professional requirement:
? ? 10 years of involvement in drug development spanning clinical activities in Phases II/IV or comparable experience in industry.
? ? 5 years of demonstrated leadership and accomplishment in all aspects of conducting clinical trials (e.g., planning, executing, reporting and publishing), or section of clinical programs in a global/matrix environment (including remote) in pharmaceutical industry.
? ? 5 years people management experience required, this may include management in a matrix environment. Global people management experience desirable.
? Strong management, interpersonal, communication, negotiation and problem solving skills.
? Considerable organizational awareness (e.g., inter-relationship of departments, business priorities), including significant experience working cross-functionally and in global teams.
? Medical/scientific and operational expertise appropriate to the program.
? Demonstrated technical knowledge and innovation in clinical development study designs that provide relevant evidence to decision-makers.
? Prior history with post-marketing/brand optimization studies to obtain evidence of brand value and support commercialization activities preferred. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Global Category Manager - Health Economics & Outcomes Research |
| University (Bachelors) in a scientific field (Preferred) or BS in other field with applicable experience, relevant advanced degree in scientific/clinical experience
Graduate Degree in Business (Preferred)
Certified Purchasing Manager (CPM) or equivalent experience
1. Broad business experience to include purchasing/sourcing in progressive companies where best in class practices are employed.
2. Experience with database sources for health economics and outcomes research, and experience in sourcing pharmacovigilance/medical safety
3. Strong leadership and effective business partnering capabilities.
4. Proven ability to lead cross-functional teams in a complex organization |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
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