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Search Jobs by Category
| BD (Becton, Dickinson and Company) |
Woburn |
MA |
11/20/2009
|
| Bioanalytical Chemist |
| See above |
| BD (Becton, Dickinson and Company) |
Woburn |
MA |
11/20/2009
|
| Manufacturing Supervisor |
| See above |
| BD (Becton, Dickinson and Company) |
Woburn |
MA |
11/20/2009
|
| Quality Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Wilson |
NC |
11/20/2009
|
| Manufacturing Technician II (Packaging) |
| See above |
| BD (Becton, Dickinson and Company) |
Wilson |
NC |
11/20/2009
|
| Manufacturing Technician I |
| See above |
| BD (Becton, Dickinson and Company) |
Wilson |
NC |
11/20/2009
|
| Automation Technician II |
| See above |
| BD (Becton, Dickinson and Company) |
Wilson |
NC |
11/20/2009
|
| Facilities Maintenance Technician I |
| See above |
| BD (Becton, Dickinson and Company) |
Wilson |
NC |
11/20/2009
|
| Information Technology Senior Specialist |
| See above |
| BD (Becton, Dickinson and Company) |
Wilson |
NC |
11/20/2009
|
| Inspection Technician II |
| See above |
| BD (Becton, Dickinson and Company) |
Wilson |
NC |
11/20/2009
|
| Manufacturing Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Wilson |
NC |
11/20/2009
|
| Manufacturing Associate I |
| See above |
| BD (Becton, Dickinson and Company) |
Wilson |
NC |
11/20/2009
|
| Validation Technician II |
| See above |
| BD (Becton, Dickinson and Company) |
Wilson |
NC |
11/20/2009
|
| Production Planner/Buyer |
| See above |
| BD (Becton, Dickinson and Company) |
Wilson |
NC |
11/20/2009
|
| Quality Control Microbiologist |
| See above |
| BD (Becton, Dickinson and Company) |
Wilson |
NC |
11/20/2009
|
| Quality Systems Leader |
| See above |
| BD (Becton, Dickinson and Company) |
Wilson |
NC |
11/20/2009
|
| Tech Transfer Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Wilson |
NC |
11/20/2009
|
| Validation Engineer |
| See above |
| Agilent Technologies, Inc. US |
Wilmington |
DE |
11/20/2009
|
| Marketing Technical Writer Intern |
| Qualifications:
- Proficient with Microsoft Word and and PowerPoint
- Strong verbal and technical writing skills.
- Strong typing skills
- Proficient and comfortable using internet and web-based tools.
cb~11/03/2009 |
| Agilent Technologies, Inc. US |
Wilmington |
DE |
11/20/2009
|
| Marketing Program Manager |
| ? Undergraduate degree in Marketing or Business Administration. Strongly prefer chemistry or Biological Sciences degree.
? Minimum of 7 years of demonstrated results in a marketing role or relevant experience
? Worldwide experience developing outbound marketing programs to drive demand for new and existing products, as well as encourage repeat purchasing
? Well developed strategic thinking skills, project management skills, experience working with outside suppliers, a proven track record of measuring and enhancing program effectiveness, strong initiative, and the ability to work with a diverse group of individuals are critical.
? Demonstrated experience developing justifications for marketing investments (ROI analysis)
? Demonstrated results orientation, including developing fact-driven, business goal-focused plans that align with strategic objectives
? Effective project management and organizational skills
? Clear and compelling writing skills; strong oral communication skills; strong content presentation skills
? Ability to work collaboratively with a diverse group of individuals cross-organizationally, cross-functionally and within a global matrix
? Strong initiative and creativity
? Experience in relationship marketing, retention, and loyalty strategies using a range of direct marketing channels
? Proven ability to understand the needs and buying influences of a scientific target audience |
| Agilent Technologies, Inc. US |
Wilmington |
DE |
11/20/2009
|
| Customer Account Specialist |
| ? Bachelor of Arts or Bachelor of Science degree
? Ability to travel
? Relevant customer experience
Geo Location: Wilmington, DE
~cb~11/11/09 |
| Agilent Technologies, Inc. US |
Wilmington |
DE |
11/20/2009
|
| Online Sales Specialist - Intern |
| Completion of sophomore/junior/senior year towards a BA/BS in Chemistry, Biochemistry, or related science degree
Would also consider Business, Marketing or similar discipline
Proficiency in the use of Microsoft Office - Excel, Word, Outlook
Strong interest in interacting directly with customers (via phone, email)
Excellent verbal, written and phone communications skills
Must be a team player with ability to work in a fast paced, dynamic team environment |
| 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. |
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. |
| Merck & Co., Inc. |
Whitehouse Station |
NJ |
11/19/2009
|
| Global Payroll Lead |
| Required:A minimum of ten (10) years experience working in a business environment. A minimum of five (5) years managing a global payroll function/operation. A minimum of five (5) years managing people and vendors. Desired:A minimum of two (2) years payroll experience in 2 regions outside the US Business process improvement experience (Six Sigma preferred). Knowledge of ERP (SAP preferred). Certified Payroll Professional (CCP) designation. A minimum of 2 yrs experience working in a shared services environment. Fluency in French. Broad understanding and knowledge of HR business processes. Solid oral and written communication and interpersonal skills. Education Requirement:Bachelor's degree required, masters preferred. A concentration in HR highly desired. 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 # HUM001307. 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. |
Whitehouse Station |
NJ |
11/19/2009
|
| Co-Op, Graphic Designer- Labeling Services |
| This position requires candidate to be currently in pursuit of a minimum of a Bachelor's degree in graphic arts, package design, or related field. Experience in a pharmaceutical, food, cosmetic labeling or packaging design and development group is a plus. Demonstrated proficiency in the Macintosh Operating System and in graphic arts application software (Creative Suite, including Adobe Acrobat/Distiller, InDesign, and Illustrator) required to produce fully-composed, electronic artwork for printed packaging components (labels, cartons, etc.) is required. Candidate must be able to work full time for a minimum of six months. Successful candidate will display accurate and thorough work. Shows good judgment with thought and detail. Effective communication skills (oral and written) as well as strong organizational skills essential. Strong interpersonal skills and the ability to work well with others and provide significant contributions as a member of a team. Demonstrated flexibility and handle multiple tasks well under pressure. 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 # QUA001917. 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 |
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! |
| Agilent Technologies, Inc. US |
Westlake Village |
CA |
11/20/2009
|
| Field Service Engineer- Westlake Village |
| Description : Representative for the Life Sciences and Chemical Analysis Group (LSCA) of Agilent Technologies. Responsibilities include on-site installation, customer training, repair and troubleshooting of hardware, and provide routine preventative maintenance, qualifications, and verification services. Typical products include Liquid Chromatographs, Gas Chromatographs, Mass Spectrometers, UV/VIS Spectrophotometers and Data Systems. Job focus will be on customer satisfaction by providing customers with high quality services. Other responsibilities include adherence to environmental health and safety guidelines, managing parts, coordinating resources, training, organization, providing feedback to manufacturing divisions, working with sales forces, and maintaining up to date technical knowledge for assigned products. Will be part of a team that delivers on-site services at a major account.
Agilent Technologies is the world's premier measurement company. Agilent provides core electronic and bio-analytical measurement tools to engineers, service providers, researchers and scientists in the electronics, communications, life science research, environmental and petrochemical industries.
~cb~11/17/09 |
| Agilent Technologies, Inc. US |
Westlake Village |
CA |
11/20/2009
|
| Field Service Engineer- Westlake Village |
| Description : As the Field Technical Support Representative for a high tech growth business serving the Chemical Analysis and Life Science markets, your primary responsibilities will include: Installation, repair and qualification services for Agilent and non-Agilent analytical instruments (LC/GC/MS) products for customers, on-site. Provides service in accordance to a maintenance contract, which may involve a managed service arrangement. Will be part of a team that delivers services on-site for large volume customers.
Perform the duties of a Customer Service Representative for the Life Sciences and Chemical Analysis Group (LSCA) of Agilent Technologies. Responsibilities include on-site installation, customer training, repair and troubleshooting of hardware, and provide routine preventative maintenance, qualifications, and verification services. Typical products include Liquid Chromatographs, Gas Chromatographs, Mass Spectrometers, UV/VIS Spectrophotometers and Data Systems. Job focus will be on customer satisfaction by providing customers with high quality services. Other responsibilities include adherence to environmental health and safety guidelines, managing parts, coordinating resources, training, organization, providing feedback to manufacturing divisions, working with sales forces, and maintaining up to date technical knowledge for assigned products.
Agilent Technologies is the world's premier measurement company. Agilent provides core electronic and bio-analytical measurement tools to engineers, service providers, researchers and scientists in the electronics, communications, life science research, environmental and petrochemical industries.
~cb~11/05/09 |
| 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
|
| 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 |
| 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. |
| 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. |
| 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. |
| 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. |
| 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. |
| 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 |
| 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. |
| 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 |
| 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 |
| Johnson & Johnson Family of Companies |
West Palm Beach |
FL |
11/19/2009
|
| West Palm Beach, FL: Territory Business Manager Vistakon, Division of Johnson & Johnson Vision Care, Inc. |
| To be considered for this role, a Bachelor's Degree is required. A minimum of 3 years of business-to-business and/or medical sales experience is also required. 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. 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 |
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! |
| Biogen Idec, Inc. |
Wellesley |
MA |
11/20/2009
|
| Manager, Regional Meeting Planning |
â?¢ Leadership skills highly important: must be able to delegate, deliver feedback, and make quick, effective decisions
â?¢ Interpersonal skills highly important: must be able to motivate team, listen to team ideas, and â??readâ? people
â?¢ Communication skills: must be able to communicate with all types of personalities
â?¢ Meeting planning, event planning experience
â?¢ Must have excellent customer service skills
â?¢ Professional experience for at least 10 years
â?¢ 2-3 years of managment experience preferred |
| Biogen Idec, Inc. |
Wellesley |
MA |
11/20/2009
|
| Director, Commercial Services, Customer and Partner Services |
| Healthcare industry professional with 10 years of overall experience and 5+ years specific experience leading analytical and contract management programs. Healthcare, pharmaceutical or biotechnology industry related experience preferred. Well developed computer and desktop management skills. Ability to lead in a fast paced, multi-task environment with responsibilities that are diverse. Candidate must have excellent communication, interpersonal and organizational skills. Ability to budget effectively and monitor compliance with budget. |
| Biogen Idec, Inc. |
Wellesley |
MA |
11/20/2009
|
| National Sales Director - East |
â?¢ 5 years of successful sales management experience in the pharmaceutical or biotech industry.
â?¢ Must have professional experience outside of sales, such as Marketing, Managed Markets
â?¢ Neurology or Specialty sales experience is highly desirable.
â?¢ Ability to work in close collaboration with multiple departments, including sales and marketing to align objectives
â?¢ Experience with systematic approach to both selling & sales procedures is needed.
â?¢ Strong leader with effective coaching and team building skills
â?¢ Solid negotiation, oral and verbal communication, organizational, presentation and analytical skills required.
â?¢ Ability and willingness to travel up to 60% of the time.
â?¢ There is flexibility as to where this position can geographically reside but it must be based within the Northeast/Mid Atlantic area |
| Biogen Idec, Inc. |
Wellesley |
MA |
11/20/2009
|
| Senior Manager, Marketing - Tysabri |
â?¢ Minimum 5 plus years commercial health care / prior marketing experience
â?¢ Solid understanding of key marketing principles
â?¢ Ability to manage external brand agencies and vendors on a day-to-day basis and
â?¢ Ability to manage promotional budgets
â?¢ Understand process in obtaining approval for promotional pieces materials through the medical, regulatory and legal promotional review process
â?¢ Excellent planning, analysis, project and budget management skills, with experience managing multiple projects against a timeline
â?¢ Strong interpersonal skills and the ability to work and manage cross-functional teams
â?¢ Demonstrates understanding of Pharma/Biotech commercial products, (BIIB and relevant competitor product knowledge), market dynamics and practice settings
â?¢ Detail oriented, strong quantitative and analytical ability
â?¢ Ability to understand and communicate highly scientific and technical medical information
â?¢ Must possess excellent verbal and written communication skills including strong presentation skills
â?¢ Demonstrated success in persuasion, influence, and negotiation skills
â?¢ Demonstrated business acumen
â?¢ Ability to travel up to 25%
â?¢ Prior field sales and CRM experience preferred |
| New England Research Institute |
Watertown |
MA |
11/19/2009
|
| Senior Clinical Data Manager II |
|
•BA/BS plus 5 years of data management experience or MPH plus 3 years of data management experience preferred;
•Must have prior experience in clinical trails and comprehensive knowledge of FDA, ICH, GCP, 21 CFR Part 11 regulatory requirements;
•Experience with data management software such as Inform, E-Clinical, Clinical, ClinTrial or other DMS packages;
•Ability to coordinate and monitor the quality of research data collected;
•Demonstrated GCDMP knowledge required, CDM certification preferred;
•Strong verbal and written communication and Must be team oriented.
If interested, please send your resume and cover letter to Human Resources at humanresources@neriscience.com or visit us at www.neriscience.com
__
NERI is an Equal Opportunity/Affirmative Action Employer M/F/D/V
|
| New England Research Institute |
Watertown |
MA |
11/19/2009
|
| Senior Data Manager |
|
•BA/BS plus 5 years of data management experience. MPH plus data management experience preferred.
•Must be proficient in MS Office applications;
•Strong verbal and written communication;
•Ability to multi-task;
•Must be team oriented;
•Experience with data management software such as Inform, E-Clinical, Clinical, ClinTrial or other DMS packages;
If interested, please send your resume and cover letter to Human Resources at humanresources@neriscience.com or visit us at www.neriscience.com
NERI is an Equal Opportunity/Affirmative Action Employer M/F/D/V |
| New England Research Institute |
Watertown |
MA |
11/19/2009
|
| Senior Biostatistician |
|
•PhD required: Minimum degree of MS in Statistics with PhD in appropriate life science (eg; biology, zoology) or MS in life science with PhD in statistics;
•Experience in designing assay development experiments and/or analyzing lab data working as a statistician;
•Ability to write sections of collaborative manuscripts and/or full papers on study design and methodological issues;
•Excellent communication skills---both oral and written;
•Minimum 7 years of experience beyond PhD program;
•Experience working in clinical research and working on project teams;
•Ability to mentor junior level statisticians;
•Ability to communicate directly with investigators both inside and outside of NERI on matters related to study design and results, select appropriate statistical methods and conduct complex analyses.
If interested, please send your resume and cover letter to Human Resources at humanresources@neriscience.com or visit us at www.neriscience.com
__
NERI is an Equal Opportunity/Affirmative Action Employer M/F/D/V
|
| New England Research Institute |
Watertown |
MA |
11/19/2009
|
| Data Manager II |
|
•BA/BS degree in public health, computer science or related field. Masters degree preferred
•2-4 years experience with electronic data capture systems, spreadsheets and word. Experience with Oracle and SQL preferred
•Knowledge of statistical software
such as SAS helpful;
•Proven ability to coordinate and monitor the quality of data
•Experience developing training and procedures manuals;
•Previous experience in a clinical trial environment is preferred.
If interested, please send your resume and cover letter to Human Resources at humanresources@neriscience.com or visit us at www.neriscience.com
__
NERI is an Equal Opportunity/Affirmative Action Employer M/F/D/V
|
| The HR Team, LLC |
Washington DC |
DC |
11/19/2009
|
| DDMAC Regulatory Professionals |
|
| Biogen Idec, Inc. |
Washington DC |
DC |
11/20/2009
|
| Research & Support Analyst, Government Relations |
| 3-5+ years of previous relevant and related experience |
| Johnson & Johnson Family of Companies |
Washington |
DC |
11/19/2009
|
| LAB SPECIALIST (WASHINGTON, DC 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.This position will be based in the Washington, DC 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 |
Washington |
DC |
11/19/2009
|
| Clinical Manager (Certified Diabetes Educator) - Washington, DC |
| A minimum of AS degree is required. A minimum of a RN or RD is required. BSN, MSN, or Pharm D is preferred. Certified Diabetes Educator (CDE) with one year of experience is required. Certified insulin pump trainer is preferred. Prior patient care experience is preferred. Knowledge of insulin pump therapy and management of patient blood glucose levels is preferred. Experience coordinating and conducting diabetes education programs to patients, physicians, and health care professionals is preferred. Previous computer experience with MS Office 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 |
| Johnson & Johnson Family of Companies |
Warsaw |
IN |
11/19/2009
|
| Quality Engineer II |
| A minimum of a Bachelors Degree, preferably in a technical discipline, or a minimum of 2+ years of Engineering or Quality experience related to this role is required. A minimum of 2+ years experience within a regulated environment is required, or 1+ year experience in a regulated environment with an advanced degree. Experience in an FDA regulated environment is an asset. Process Excellence, ASQ, Lean Manufacturing training and/or certifications are an asset. Process validation and verification activity experience is an asset. Risk analysis techniques, including FMEA (Failure Modes and Effects Analysis) or other methods, is required. Problem solving techniques including root cause analysis and cause and effect analysis are an asset. Statistical techniques and methods are an asset. Blue print reading and interpretation including Geometric Dimensioning and Tolerancing (GD&T) is an asset. Must have strong negotiation skills and the ability to apply good manufacturing/laboratory practices (GMP and GLP). Working knowledge of QSR and ISO 13485 (ISO9001/EN46001) quality system requirements are an asset. Prior project management experience would be preferred. Working knowledge of Microsoft Word and Excel are required, with Access, Project, and PowerPoint knowledge an asset. Excellent written and oral communication skills will be required. The ability to work independently and partner with a cross-functional team is required. The qualified candidate for this hands-on position should be able to use Quality Engineering principles, tools, and practices to develop and optimize systems and processes that are aligned with the overall business and quality vision. Will require the ability to lift up to 25 pounds. This position will require 10-20% 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! Due to technical upgrades, this requisition is replacing requisition # 0901213. Any candidates who have already applied to requisition # 0901213 are already being considered, therefore, you do not need to apply. |
| Johnson & Johnson Family of Companies |
Warsaw |
IN |
11/19/2009
|
| Senior Clinical Research Associate (in-house) |
| A minimum of a BS/BA or equivalent with 5 years clinical research experience, or a minimum 3 years experience with advanced technical degree. Advanced degree preferred. Certification from recognized professional organization (i.e. ACRP, SoCRA) preferred. Experience in orthopedics and/or orthopedic clinical trials is preferred. Experience monitoring clinical trials is required. A thorough understanding of the clinical trial process and guidelines/regulations associated is required. Experience mentoring and/or training others is preferred. Approximately 25% domestic and international travel is required. |
| BD (Becton, Dickinson and Company) |
Waltham |
MA |
11/20/2009
|
| Manufacturing Technician - Production |
| See above |
| BD (Becton, Dickinson and Company) |
Waltham |
MA |
11/20/2009
|
| Production Operator I |
| See above |
| BD (Becton, Dickinson and Company) |
Waltham |
MA |
11/20/2009
|
| Production Operator II |
| See above |
| Biogen Idec, Inc. |
Waltham |
MA |
11/20/2009
|
| Clinical Trial Manager |
â?¢Typically requires at least 5+ years of global drug development with experience managing clinical projects within time, budget, and quality expectations.
â?¢Experience in hematology/oncology clinical research and development very desirable, especially in the areas of hemophilia and clotting disorders.
â?¢NDA/BLA or MAA experience desirable, particularly within an orphan/rare disease therapeutic area.
â?¢Thorough knowledge of GCP, ICH guidelines and awareness of global regulatory requirements/differences for clinical development.
â?¢Detail and process oriented, with excellent project management skills, including risk assessment and contingency planning.
â?¢Demonstrated leadership, communication, and organizational skills, along with problem solving, conflict resolution, and team building skills.
â?¢Proven excellence in cross-functional matrix and/or cross-cultural partnership setting preferred. |
| Biogen Idec, Inc. |
Waltham |
MA |
11/20/2009
|
| Associate Scientist, Molecular/Cell Biology and Assay Support |
A minimum of 2-3 years of relevant experience. Excellent communication skills are essential and the individual should possess the ability to work well within a team environment.
Job title shall be commensurate with experience |
| Biogen Idec, Inc. |
Waltham |
MA |
11/20/2009
|
| Associate Director, Global Hemophilia Marketing |
Seasoned marketing professional, with at least 8 years of pharmaceutical commercial experience, including global marketing and market research in a specialty therapeutic area.
Experience in the following is a significant plus:
o hemophilia commercial marketing and/or sales
o execution on pre-launch and launch activities in hemophilia or specialty markets
o health economics strategy and execution |
| Biogen Idec, Inc. |
Waltham |
MA |
11/20/2009
|
| Director, Global Hemophilia Marketing |
Seasoned marketing professional, with at least 10 years of pharmaceutical commercial experience, including development and execution of a brand plan in a specialty market.
Experience in the following is a significant plus:
o hemophilia commercial strategy development
o execution on pre-launch and launch activities in hemophilia or specialty markets
o health economics expertise
o build out of infrastructure in a specialty therapeutic area new to the employer |
| Biogen Idec, Inc. |
Waltham |
MA |
11/20/2009
|
| Scientist II |
â?¢3-5 years of industry experience in (peptide/protein) analytical chemistry in a research/product development setting.
â?¢Understanding and hands-on experience with a wide range of analytical chemistry techniques: HPLC (reversed-phase, size-exclusion, ion exchange), Electrophoresis (SDS-PAGE/IEF/CE), Protein Sequencing, Peptide Mapping, Carbohydrate Analysis and Mass Spectrometry.
â?¢Knowledge and experience with amino acid post-translational modifications.
â?¢Understanding and hands-on experience with biophysical techniques: ITC and Light Scattering
â?¢Excellent oral, written and interpersonal communication skills and an ability to work across scientific disciplines.
â?¢Experience with FDA/ICH guidelines.
â?¢Knowledge of statistics and the ability to interpret experimental data to summarize the key findings.
â?¢Meticulous attention to detail in following procedures, preparing written documentation and execution of experiments.
â?¢Perform complex assays and investigate/troubleshoot assay problems. |
| Biogen Idec, Inc. |
Waltham |
MA |
11/20/2009
|
| Director, Finance Syntonix |
Qualifications:
â?¢ Significant financial management experience ranging from business unit level strategic planning to detailed budgeting and decision support.
â?¢ High level of business acumen with the ability to identify key issues and questions and explain to others with diverse functional backgrounds.
â?¢ Excellent informal leadership skills with the ability to influence peers in business line functions.
â?¢ Experience working across cultures and companies to develop effective relationships and processes.
â?¢ Effective communicator with the ability to tailor message and delivery to both technical and senior audiences. |
| Biogen Idec, Inc. |
Waltham |
MA |
11/20/2009
|
| Director, Product Development |
At least 10 years of biotech/pharmaceutical industry experience, including in program management and/or clinical development. An understanding and command of topics across manufacturing, regulatory and commercial functions is critical to success in the role. Ability to navigate a corporate organization and manage a collaboration partner with diplomacy are essential skills.
Experience in the following is a significant plus:
o hemophilia program leadership
o clinical development in hemophilia and/or in a global clinical trial
o commercial or regulatory responsibility for a program in clinical development |
| Biogen Idec, Inc. |
Waltham |
MA |
11/20/2009
|
| Clinical Program Leader |
â?¢Typically requires at least 8+ years of global drug development with experience managing clinical projects within time, budget, and quality expectations.
â?¢Experience in hemophelia, thrombosis and/or oncology clinical research and development is very desirable
â?¢NDA/BLA or MAA experience desirable, particularly within an orphan/rare disease therapeutic area.
â?¢Thorough knowledge of GCP, ICH guidelines and awareness of global regulatory requirements/differences for clinical development.
â?¢Detail and process oriented, with excellent project management skills, including risk assessment and contingency planning.
â?¢Demonstrated leadership, communication, and organizational skills, along with problem solving, conflict resolution, and team building skills.
â?¢Proven excellence in cross-functional matrix and/or cross-cultural partnership setting preferred. |
| Biogen Idec, Inc. |
Waltham |
MA |
11/20/2009
|
| Associate Scientist |
| A minimum of 3+ years of industrial research experience. The successful candidate should be responsible, motivated, flexible, a good team-player, have excellent oral and written communication skills, be able to collaborate with cross-functional teams. |
| Biogen Idec, Inc. |
Waltham |
MA |
11/20/2009
|
| Head of Human Resources, Syntonix |
Ten to fifteen years (Post University) experience in progressively responsible roles in HR, including HR business partner or generalist role supporting a multi-function business with global scope. Experience working within both small and large company environments is a significant plus.
Possesses the business maturity and interpersonal savvy to work with senior leaders, including Executive Committee members, as well as the sensitivity to work with line employees.
Track record of driving creative solutions within a dynamic environment and the ability to lead and create positive change.
Proven ability and eagerness to achieve results by working as part of a management team is essential. To develop the trust and confidence of key line and HR staff, the candidate should have strong leadership abilities (e.g., be credible, consultative, and persuasive).
Preference will be given to candidates with experience in different HR functions, and to those with experience in a highly matrixed environment.
Individuals with demonstrated leadership capabilities in line management roles are also highly desirable, as are candidates with biotechnology and/or pharmaceutical experience. |
| sanofi pasteur |
Ventura |
CA |
11/19/2009
|
| Vaccine Sales Representative - Ventura, CA |
| 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 |
| Boston Scientific |
Valencia |
CA |
11/19/2009
|
| Marketing Manager |
| Experience:
· Prefer minimum of 3 years experience in a medical-related industry in a product management, sales or marketing position with product launch experience.
· Field medical sales, technical and/or marketing communications experiences a plus.
SPECIALIZED KNOWLEDGE & SKILLS:
· Must have excellent communication skills, including the ability to listen to clinical and customer needs, prioritize needs/requirements and communicate them to cross-functional teams, including physicians.
· Must have exceptional leadership, presentation, negotiation and interpersonal skills, particularly in working effectively as a member of a team.
· Must be able to work in a fast paced environment and foster constructive relationships with internal and external customers.
· Must have excellent and professional written and verbal skills.
· Must have excellent analytical skills.
· Must have good presentation skills.
EDUCATION and TRAINING:
· Bachelor’s degree
· MBA preferred
PHYSICAL ENVIRONMENT / WORKING CONDITIONS:
· Must have the ability to handle the stresses of 25% or more travel schedule. Ability to independently manage a moderate travel schedule. Ability to be flexible in working extended schedules, including some weekends.
RESPONSIBILITY FOR PERSONNEL:
Direct Supervision: None
Indirect Supervision: None
INTERNAL CONTACTS: All levels of Sales, Engineering, Management staff, department heads, Marketing, Purchasing, Finance, Human Resources, QA, Regulatory and Clinical staff.
EXTERNAL CONTACTS:
Vendors: Vendors for all types of marketing services used in the development and promotion of medical devices; specifically, advertising agencies, market research firms, sales training organizations, graphics developers, etc.
Consultants: Scientific and health care industry consultants.
Customers: Clinicians (Referring Physicians, Implanting Physicians, Allied Health Care Providers), Hospitals and Hospital Systems, Patients, Payer Organizations, etc.
Other: University Professors and Research groups working in the Bioengineering field and the Implantable Device field.
Boston Scientific is an Equal Opportunity Employer, EEO/AA
|
| Astellas Pharma, Inc. |
Valdosta (1P030203) |
GA |
11/19/2009
|
| Professional Representative, PCP - Valdosta/Albany, GA |
| THE SUCCESSFUL CANIDATE FOR THIS ROLE WILL HAVE:- A Bachelor Degree- Excellent communication, facilitation and presentation skills- Can do approach and very high motivational and persuasion skills- Some experience (1 year) with business-to-business sales If you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you. |
| 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. |
| Johnson & Johnson Family of Companies |
Tupelo |
MS |
11/19/2009
|
| Lab Specialist (Tupelo, MS) |
| 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 Tupelo, MS 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! |
| BD (Becton, Dickinson and Company) |
Teterboro |
NJ |
11/20/2009
|
| Pilot/Aircraft Captain Corporate Flight Department |
| See above |
| Johnson & Johnson Family of Companies |
Taunton |
MA |
11/19/2009
|
| Manager, Clinical Research |
| Minimum of a Bachelors degree in Science or related Health Field is required in this role with a Masters Degree in Science/related Health Field preferred. Also preferred is an, MBA. 10 years industry experience with 7 years experience in the Pharmaceutical or Medical Device industries is required. Strong leadership skills and the ability to develop successful strategies while fully understanding the complex environment of the assigned program. Experience in multiple functional areas strongly preferred (Clinical, Marketing, R&D, Sales)Significant project management experience with cross-functional, cross-company and international project teams. Clinical trial experience is strongly preferred and international trial experience is a plus.Strong ability to communicate clinical information (concepts and results) in oral and written communication to experts (e.g., KOL, FDA reviewers) and to product development team members (e.g., clinicians, marketing personnel, engineers)Understanding of the contribution of scientific and medical affairs goals to company business strategiesExperience drafting or reviewing technical documents (e.g., Clinical protocols/reports, design FMEAs, IOVVs). Appropriate knowledge of GMP, GCP and regulations required.Proven insight into the integration of science, regulatory, and business principles as it pertains to the successful development of multi-center clinical studies.Understanding of reimbursement landscape in the US and OUS is beneficial.Prior experience in strategic roles, along with excellent written and oral communication skills, and experience presenting to senior management also required.Ability to foster a strong collaborative team environmentDemonstrated ability to collaborate and work effectively in a fast-paced matrix environmentDemonstrated negotiation and conflict resolutions skills, including the ability to influence without clear reporting authorityStrong professional diplomacy Strong organizational skills (e.g., able to manage multiple institutions and/or projects). 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 |
Taunton |
MA |
11/19/2009
|
| Manager, Clinical Operations |
| Requires a BS or BA in a relevant scientific discipline and minimum 8 years relevant clinical experience in the pharmaceutical or medical device industry.Excellent interpersonal skills, and demonstrated ability to lead is required.Experience in managing staff as well as mentoring and developing junior staff.Strong communication and influence skills and ability to create a clear sense of direction is necessary. Must have a demonstrated ability to successfully develop, implement, manage and complete clinical trials.Thorough knowledge and understanding of FDA and/or GCPs is required and EMEA Regulations, ICH Guidelines, and governing the conduct of clinical trials is an asset. Experience in developing RFPs and selection and management of CROs/vendors.Ability to examine functional issues from a broader organizational perspective.Ability to participate in and/or lead departmental or interdepartmental strategic initiatives under limited supervision.Ability to meet on time delivery and deadlines and expediting others is a requirement.Functional expertise to initiate, author, or contribute to SOP development, implementation, and trainingIf 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 |
Taunton |
MA |
11/19/2009
|
| Master Data Management Specialist - Casual Part-Time |
| A minimum of an Associate's Degree is required. A Bachelors degree would be preferred. A Degree in Business, Finance, Economics, IT or related field would be preferred. A minimum of 3 years related business experience required. Previous experience in a health-related service industry and/ or a regulated industry is highly desirable. Experience working with customer databases desired. Experience with Cognos or other reporting tools desired. Strong MS Excel skills required. Proficiency utilizing the Microsoft Office Suite (Word, PowerPoint, Outlook etc) required. Prior experience creating and writing reports preferred. Experience with MS Access or equivalent experience preferred. The candidate must possess excellent listening, verbal and written 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. Excellent time management and organizational skills and the ability to effectively prioritize are required. This is a casual part-time position (19.5 hours) - candidate must be willing to work 19.5 hours a week. The schedule will be determined by the Manager as per business needs. This position will be based in Raynham, MA. 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 |
Tampa |
FL |
11/19/2009
|
| Tampa, FL- 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 |
Tampa |
FL |
11/19/2009
|
| Tampa, FL: 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! |
| 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! |
| 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. |
| 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. |
| 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 |
St. Louis |
MO |
11/19/2009
|
| St. Louis, MO (East): 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 |
St. Louis |
MO |
11/19/2009
|
| St. Louis, MO: Clinical Sales Representative - 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 |
Springfield |
MA |
11/19/2009
|
| Worcester, MA: Energy Sales Specialist - 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 |
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 |
South San Francisco |
CA |
11/19/2009
|
| Director, Medical Writing - Janssen AI, LLC |
| A minimum of a Bachelor's degree in a science or communication discipline with a minimum of 10 years medical writing experience in the clinical or laboratory setting, OR an Advanced Degree with 7 years medical writing experience in a clinical or laboratory setting preferred. Excellent leadership and management experience. Good understanding of experimental methods, research design, and statistical analysis. Ability to analyze medical data and interpret its significance within a pharmaceutical setting. Ability to interpret, analyze, and present statistical data obtained in a clinical trial. Advanced scientific, technical reading, writing and editing skills. Excellent oral communication skills. Proficient computer and word processing skills. Use of templates and experience with document management systems. Up to 5% yearly travel may be required (International as well as Domestic). 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 |
South San Francisco |
CA |
11/19/2009
|
| Head of Biometrics (Senior Director) - Janssen AI, LLC |
| A Ph.D. degree in Biostatistics or closely related field is required. A minimum of 15 years of pharmaceutical experience with at least 5 years of management level experience. International experience is strongly desired. Excellent verbal and written communication skills. Must have a working knowledge of filing regulatory documents and complex statistical methods that apply to all phases of clinical trials. Strong attention to detail and accuracy is a must. Ability to effectively present information to senior management, regulatory authorities, public groups, and other departments. Demonstrated ability to integrate planning efforts across departments to ensure organizational effectiveness. Ability to cultivate internal and external relationships based on trust and respect in anticipation of future working relationships. Demonstrated ability to proactively maximize relationships to enable successful collaboration. Demonstrated ability to facilitate a beneficial resolution of conflict. Ability to articulate a clear vision and help others understand their relationship between their roles, the roles of others and the overall goals of the organization; ability to articulate the reason behind organizational changes and demonstrate flexibility, energy and resilience throughout change efforts. Demonstrated ability to work cooperatively within and outside the organization to accomplish the best outcomes; ability to work in diverse teams to optimize decision-making. Demonstrated ability to provide coaching and feedback to foster professional development while also supporting business goals. 10-15% International and Domestic travel is required. |
| Johnson & Johnson Family of Companies |
South San Francisco |
CA |
11/19/2009
|
| Manager of Financial Reporting and Analysis - Janssen AI, LLC |
| A minimum of a Bachelors Degree in Finance or Accounting. A minimum of 5 years financial experience required. Experience working within a pharmaceutical industry experience preferred. Excellent PC skills and experience including SAP, Excel and PowerPoint. Strong analytical ability. Exceptional communication and interpersonal skills, including oral and written. Demonstrated ability to perform in an environment that emphasizes teamwork. Demonstrated ability to lead a process with minimal or no supervision. Demonstrated capacity to effectively manage multiple and frequently changing priorities. High degree of accuracy with attention to detail and ability to meet strict deadline. 10% Domestic and International Travel is required. |
| Johnson & Johnson Family of Companies |
South San Francisco |
CA |
11/19/2009
|
| Manager, Information Technology and Facilities Management - Janssen Al, LLC |
| A minimum of a High School Diploma is required, a Bachelors degree is preferred. Project Management Professional (PMP) Qualification is preferred. Experienced in I.T. support for Facilities/Operations groups is required. Experienced in I.T. and Facilities change management with a in Pharma R&D organization is required. Experience with administration and coordination skills across peer groups is required. Knowledge of J&J systems, J&J standards and processes is preferred. 10-20% International and Domestic travel is required. |
| Johnson & Johnson Family of Companies |
South San Francisco |
CA |
11/19/2009
|
| Director, Customer Insight and Market Development - Janssen AI, LLC |
| A Minimum of a BA/BS is required with an advanced degree preferred. 8 or more years of progressive marketing experience is required, preferably in the consumer or devices industry. Extensive line marketing experience, senior brand responsibility, product launch experience, and team leadership is also required. The ideal candidate will have demonstrated success in establishing new markets/new paradigms. Line marketing experience demonstrating commitment to innovation through deep customer insights is preferred. Demonstrated track record participating in highly matrixed, cross-functional work teams composed of high-level managers and executives is preferred. Extensive experience accomplishing objectives through people is preferred. Position requires significant domestic and some international travel (approximately 10%). |
| Johnson & Johnson Family of Companies |
South San Francisco |
CA |
11/19/2009
|
| Strategic Marketing Director- Janssen AI, LLC |
| Bachelors Degree is required, MBA or Masters Level degree is preferred. A minimum of 10 years of progressive marketing experience in the pharmaceutical industry is required. Launch experience with a pharmaceutical or bio-pharmaceutical product, or experience in a lead role managing a marketed pharmaceutical or bio-pharmaceutical product is also required. Experience in strategic marketing, market development and new product/drug development processes are required. Extensive knowledge of clinical and regulatory development desired. Experience partnering with pharmaceutical R&D teams is required. Strong analytical skills in uncovering and analyzing problem areas/growth opportunities are required. Excellent and proven collaborative skills in developing relationships, leading highly matrixed, high performing, multi-functional cross-company teams, are required. A proven ability to create alignment across teams from multiple operating units, functions and geographies is required. Global experience is preferred. Approximately 20% domestic travel required. |
| Johnson & Johnson Family of Companies |
South San Francisco |
CA |
11/19/2009
|
| Global Marketing Director Bapineuzemab - Janssen AI, LLC |
| A minimum of a BA/BS is required with an advanced degree preferred. 10 or more years of progressive marketing experience is required, preferably in the pharmaceutical or devices industry. Extensive line marketing experience (prefer strong US experience in an infusion/biological setting), senior brand responsibility, product launch experience, and team leadership is also required. Ideally will have demonstrated success in establishing new markets/new paradigms. Minimum of 2 years strategic global marketing leadership experience. Line marketing experience demonstrating commitment to innovation through deep customer insights is key. Demonstrated track record leading highly matrixed, cross-functional work teams composed of high-level managers and executives. Experience with global R&D programs required. Extensive experience accomplishing objectives through people. Position requires significant domestic and some international travel (approximately 50%). |
| Johnson & Johnson Family of Companies |
South San Francisco |
CA |
11/19/2009
|
| Clinical Program Manager - Janssen AI, LLC |
| BS or BA in a relevant scientific discipline is required. Must possess at least 5 years of relevant clinical experience in the pharmaceutical (or similar) industry. Excellent interpersonal skills and demonstrated ability to lead is required. Experience in managing staff as well as mentoring and developing junior staff is preferred. Strong communication and influence skills and the ability to create a clear sense of direction is necessary. Must be able to resolve problems using national and international regulations and guidelines. Must have a demonstrated ability to successfully develop, implement, manage and complete clinical trials. Thorough knowledge and understanding of FDA and/or EMEA Regulations, ICH Guidelines, and GCPs governing the conduct of clinical trials is required. Experience in developing RFPs and selection and management of CROs/vendors is required. The ability to write study protocols, study reports, sections for investigator brochures and regulatory documents (e.g. IND, DNA, etc.) with little supervision is required. The ability to examine functional issues from a broader organizational perspective is required. The ability to participate in and/or lead departmental or interdepartmental strategic initiatives under limited supervision is required. Functional expertise to initiate, author, and/or contribute to SOP development, implementation and/or training is preferred. 25% travel is required, both international and domestic. |
| Johnson & Johnson Family of Companies |
South San Francisco |
CA |
11/19/2009
|
| Senior Clinical Budget Analyst - Janssen AI, LLC |
| A Bachelor's Degree is required. Working knowledge of the clinical development process and 2+ years of experience in clinical budget development and management are required. Must possess an understanding of clinical trials, regulatory affairs, quality assurance, clinical trial materials, budgeting and routine contracts. Previous experience with industry benchmarking database(s) is strongly preferred. Excellent communication skills (both oral and written) are required. The ability to work effectively in cross-functional teams is required. Strong and proven negotiation and problem resolution skills are also required. Strong business acumen and an innovative spirit are required. Strong inter-personal and collaboration skills are required. Must possess the ability to accomplish substantial tasks with minimal supervision. Experience in assisting and drafting of legal contracts and familiarity of clinical budget development and negotiation is required. |
| Johnson & Johnson Family of Companies |
South San Francisco |
CA |
11/19/2009
|
| Manager, Clinical Data Management - Janssen AI, LLC (1 of 2) |
| High School diploma required. Med Tech background preferred. BS/BA degree preferred. A background in Life Sciences is a plus. A minimum of 5+ years of data management experience within a pharmaceutical and/or health care environment required. Electronic data capture experience preferred. Experience managing external vendors is required. Knowledge of FDA regulatory requirements is strongly preferred. |
| Johnson & Johnson Family of Companies |
South San Francisco |
CA |
11/19/2009
|
| Senior Clinical Contract Analyst - Janssen AI, LLC |
| A Bachelor's Degree is required. A certificate of completion of formal course in Paralegal studies is preferred. Certification of Notary Public is a plus. Working knowledge of the clinical development process and 2+ years of experience in clinical budget development and management are required. Must possess an understanding of clinical trials, regulatory affairs, quality assurance, clinical trial materials, budgeting and routine contracts. Excellent communication skills (both oral and written) are required. The ability to work effectively in cross-functional teams is required. Strong business acumen and an innovative spirit are required. Strong inter-personal and collaboration skills are required. Must possess the ability to accomplish substantial tasks with minimal supervision. Familiarity of clinical budget development and/or negotiation is required. |
| Johnson & Johnson Family of Companies |
South San Francisco |
CA |
11/19/2009
|
| Global Marketing Director, Infrastructure - Janssen AI, LLC |
| BA/BS required; Advanced degree in business or life sciences preferred. A minimum of 10 years of progressive marketing experience is required with a proven track record of exceptional team & cross-functional leadership. Pharmaceutical industry experience is highly preferred, significant line marketing experience with senior brand responsibility, is required. Global marketing experience and launch experience is preferred. Demonstrated global mindset with the ability to assimilate complex science quickly is required. This position requires up to 25% domestic/international travel. |
| Johnson & Johnson Family of Companies |
South San Francisco |
CA |
11/19/2009
|
| Global Commercial Leader - Janssen AI, LLC |
| Bachelor's degree required; advanced degree preferred. A minimum of 14 years of progressive marketing experience preferably in the pharmaceutical or devices industry; extensive line marketing experience (prefer strong US experience in an infusion/biological setting), senior brand responsibility, product launch experience, and team leadership required. Ideally will have demonstrated success in establishing new markets/new paradigms. A minimum of 2 years strategic global marketing leadership experience required. Demonstrated track record leading highly matrixed, cross-functional work teams composed of high-level managers and executives. Experience with global R&D programs preferred. Extensive experience accomplishing objectives through people. Position requires significant domestic and some international travel. |
| 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. |
| 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. |
| 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! |
| Johnson & Johnson Family of Companies |
Somerville |
NJ |
11/19/2009
|
| Senior Engineer |
| A BS degree required. A MS degree preferred. Minimum 5 years of related engineering (related to electro mechanical devices) experience required. Experience in a highly regulated environment is highly preferred. Knowledge of ISO and cGMP regulations is required. Previous experience with leading and conducting process validation activities required. Experience with electro-mechanical manufacturing processes preferred. Competent working knowledge of DX methodologies, statistical techniques required. Good communication and presentation skills required. A certification in Process Excellence (Green Belt or Black Belt) is preferred. Competent PC literacy including CAD applications preferred. Due to technical upgrades, this requisition is replacing requisition # 0903157. Any candidates who have already applied to requisition # 0903157 are already being considered, therefore, you do not need to apply. |
| Johnson & Johnson Family of Companies |
Somerville |
NJ |
11/19/2009
|
| Principal Scientist Veterinary Surgeon - Somerville, NJ |
| A DVM/VMD (from an AVMA (American Veterinary Medical Association) approved and accredited program) or equivalent degree is required. Board Certification is strongly preferred but not required. Surgical residency training and/or industry experience (minimum 3 years in industry without residency) is required. Scientific publications are required. Experience working in a team environment is required. Highly motivated, self-starting, and strong verbal and written communication 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! |
| Johnson & Johnson Family of Companies |
Somerville |
NJ |
11/19/2009
|
| Medical Device Systems Engineer (Staff Engineer) |
| A minimum of a Bachelor's degree in Mechanical Engineering, Electrical Engineering, or equivalent discipline is required. An advanced degree is an asset. A minimum of 8+ years of overall work experience is an asset, with 5+ years of specific experience in electro-mechanical machine and/or medical device product design an asset. Experience designing electromechanical systems with software interface with practical knowledge of mechanical systems and electronics is an asset. A minimum of 2+ years working knowledge of software/development methodologies as demonstrated by an ability to develop software architecture is an asset. Knowledge of experimentation methods and statistical techniques is an asset. Knowledge of electronics manufacturing and/or mechanical component manufacturing processes is an asset. Working knowledge of FDA requirements for Class II and III medical devices is an asset. Electrical Safety and EMI/EMC standards knowledge or experience is an asset. Strong analytical skills, excellent written and verbal communication skills, strong organizational skills, and effective interface with project teams, physicians and suppliers will be needed in this role. This position will be located in Somerville, 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! |
| Johnson & Johnson Family of Companies |
Somerville |
NJ |
11/19/2009
|
| Senior Engineer |
| A minimum of a Bachelor's degree in an Engineering discipline is required. An advanced degree is an asset. A minimum of 5 years of related engineering experience in an FDA regulated environment is required. Knowledge of ISO and cGMP regulations is required. Previous experience with conducting design verification and validation testing in support regulatory submissions required. Experience with competitive benchmarking, and process qualifications is required. Engineering prototype evaluation is an asset. Project management experience required. Strong communication, and influencing skills are required. A certification in Process Excellence (Green Belt or Black Belt) is an asset. This position may require up to 25% 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! |
| Johnson & Johnson Family of Companies |
Somerville |
NJ |
11/19/2009
|
| Staff Scientist - Analytical Chemistry |
| A minimum of a Ph.D. in Polymer Science, Polymer Chemistry, or Material Science/Engineering with 5+ years of related experience, or equivalent, is an asset. Experience with materials used in the medical device industry is an asset. Experience in new product development processes is preferred. A background in polymer chemistry, processes and bulk polymer characterization techniques thereof (Thermal Analyses, Microscopy, Spectroscopy, Chromatography) is required. Must be able to combine characterization methods and/or adapt new methods in order to solve problems. A working knowledge of surface science processes and techniques is an asset. Good communication and presentation skills must be evident; patents, peer review publications and presentations is a plus. Must be able to communicate detailed polymer characterization data to a diverse group of technical and non-technical associates involved in the product development process. Strong interpersonal and leadership skills are essential. Ability to work in team environment, be further mentored by senior scientific fellows, and mentor junior staff members is necessary. This position is located in Somerville, 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! |
| Johnson & Johnson Family of Companies |
Somerville |
NJ |
11/19/2009
|
| Professional Education Director Biosurgery |
| A minimum of a Bachelor's Degree is required, scientific discipline or Masters Degree preferred. 3 years of medical device customer facing experience or relevant clinical experience required. Minimum 3 years of applicable Orthopedic, Cardiothoracic, NeuroSpine, ENT, General surgery, GYN, Urologic, Plastic and Burn surgery business unit experience andor relevant expertise required. Experience in the planning and delivery of medical device professional education programs strongly preferred. Experience managing professional education components during new product launches and global expansion preferred. Experience in project management including managing multiple complex projects, budgets and analytics preferred. 3 or more years supervisory/management or team leader experience preferred. Customer Focus, Accountability, Collaboration & Teamwork, Project/Process Management, Strategic Thinking skills required. Must have strong desire and skill sets to advance within the organization. 30-60% domestic and international travel required. |
| Johnson & Johnson Family of Companies |
Somerville |
NJ |
11/19/2009
|
| Staff Mechanical Engineer |
| A minimum of a Bachelor's degree in Mechanical Engineering, Design Engineering, Biomedical Engineering or a related discipline is required. An advanced degree is an asset. A minimum of 2+ years work experience in product design/development or manufacturing processes testing is required. Experience in design and development of medical devices is an asset. Experience in design of mechanical devices, systems and/or electro-mechanical products is an asset. Successful completion of products from concept to launch is an asset. CAD ability in Solidworks, Mechanical Desktop or equivalent design software is an asset. A general knowledge and understanding of QSR, DOE, QFD, DFMA, and FMEA is an asset. Must be able to apply and comprehend a broad range of engineering and scientific assignments as well as have demonstrated the ability to work independently and within a group. Will utilize the support of technicians also assigned to the project team. Computer literate in project planning and or data acquisition is desirable. Must be self-motivating and innovative and be able to work on multiple projects with different priorities. Extensive verbal and technical writing skills as well as proven analytical and problem solving 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! |
| Johnson & Johnson Family of Companies |
Somerville |
NJ |
11/19/2009
|
| Director, Health Economics and Reimbursement (HE&R) - Strategic Market Access North America |
| A minimum of a Masters degree in biomedical science, health service research, or economics is required. Post doctoral experience is also desirable. Health services research (health economics, outcomes research) and clinical epidemiology experience preferred. A minimum of 5 or more years experience in the Medical Device, Pharmaceutical or Health plan industry is required with track record of scientific and business impact success. Knowledge of reimbursement across treatment settings (i.e., hospital inpatient, hospital outpatient, physician's office, long term care, home health, etc.) is required. Previous reimbursement/market access experience working with health plans and payors is required; an understanding of billing and reimbursement procedures from the facility and payor perspective would be preferred. Understanding of complexities associated with the changing health care environment (i.e., fee-for-services, comparative effectiveness, federal/state health care reform risk, outmigration of care) is required. This position requires strong communication and presentation skills. Knowledge of Medicare, Medicaid, Employers and hospital operations is highly desirable. Understanding process and decision-making criteria for evaluating new technologies and for setting reimbursement rates is highly desirable. A minimum of 50% 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 |
Somerville |
NJ |
11/19/2009
|
| Senior Quality Engineer |
| A minimum of a Bachelor's degree in Engineering, Life Science, Physical Science or a related field is required, with an Advanced degree is preferred. A minimum of 4+ years of Quality Engineering experience is required. Experience in the medical device, pharmaceutical or other highly regulated industry is required. New product development experience is required. Supplier quality engineering experience is a plus. Experience with the development of Electro-mechanical devices is an asset. Knowledge of IEC 60601-1 is preferred. Knowledge of ISO and/or cGMP regulations is required. Strong knowledge in Quality Systems Regulations (QSR) preferred. ASQ certifications (CQE, CQM, CRE or CQA) is preferred. Six Sigma Green Belt or Black Belt is desired. Knowledge in Statistics, Sampling Planning, Reliability, Computer System Validation and Process Validation is an asset. Candidate must be able to communicate effectively at all levels within Quality as well as cross functionally with departments such as R&D, Operations, Purchasing, Marketing and Medical Affairs. This position may require up to 20% 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 |
Somerville |
NJ |
11/19/2009
|
| Regulatory Affairs Specialist |
| A minimum of a Bachelor's degree in Biology, Biochemistry, Immunology or a related discipline is required. A PhD degree in Biology, Biochemistry, Immunology or a related discipline is strongly preferred. A minimum of 2+ years experience in Regulatory Affairs required. Experience or exposure to the field of Biologics is required. Medical Device and Pharmaceutical experience is an asset. US Regulatory experience is required. EU and International Regulatory experience is an asset. Previous experience in regulations and submitting files for health authorities in Israel is an asset. Excellent communication skills will be necessary for this role. This position will require 10% travel and will be located in Somerville, NJ. |
| Johnson & Johnson Family of Companies |
Somerville |
NJ |
11/19/2009
|
| Staff Engineer - Polymer Processing |
| An MS or Ph.D. in Polymer Science, Chemical Engineering, Bio Medical Engineering or allied field is an asset, with 5+ years of experience in an industrial environment as a technical leader and/or project leader an asset. Adept, hands-on experimentalist background with extensive experience in polymer processing, including extrusion, fiber spinning and associated down stream processes of crystalline resins is an asset. Strong background in polymer physics, with good understanding of material characterization, structure-property and utilization towards application development is an asset. Will need the ability to work in a team-oriented environment that embraces change, risk, and flexibility and must be capable of handling multiple projects/tasks at the same time. A demonstrated ability to work independently and within a team as well as the ability to listen to customers' needs and develop solutions to meet their requirements. Experience in medical devices product/process development is an asset. Experience in bioabsorbable polymers and polymer processing technology is an asset. Knowledge of medical devices regulations is an asset. Knowledge of Design/Process Excellence (Six Sigma) is 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 |
Somerville |
NJ |
11/19/2009
|
| SENIOR DIRECTOR, REGULATORY AFFAIRS |
| A minimum of a Bachelor's degree in a scientific discipline is required, with an advanced degree is strongly preferred. A minimum 10+ years of experience in regulatory affairs or a related field is required. RAC is an asset. Direct experience with US/EU regulatory submissions is required. PMA experience or experience with PMA products is an asset. Experience successfully taking a product through development and regulatory cycle required. Proven leadership and strong people management skills will be needed. Successful track record in coordinating and experience with interacting with multiple and diverse business units required. Excellent oral and written communication skills 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 |
Somerville |
NJ |
11/19/2009
|
| Associate Director, Forecasting |
| BS or BA in business, marketing, statistics, mathematics, or related field. MBA or MS is preferred. A minimum of 8 years of progressive experience in forecasting, business analytics, finance, market research, portfolio analysis, or a related field is required. Experience in the medical device, hospital specialty, or healthcare field is preferred. Proficiency in Microsoft EXCEL, PowerPoint, CrystaBall, or Risk is required. Experience in creating market modeling and revenue forecasting is required. Working knowledge of industry primary, secondary data and / or competitive intelligence data is strongly preferred. Excellent leadership, collaboration, communication and analytical skills are required. Must be able to influence and impact others through building and defending arguments and reaching consensus of opinion. Excellent verbal and written presentation skills are required. Ability to understand and translate data into actionable information to support decision-making is required. Demonstrated success in creative problem solving and team partnership is required. Strong project management skills are required. Working knowledge of Monte Carlo simulation techniques is preferred. This position is based in Somerville, NJ. |
| Johnson & Johnson Family of Companies |
Somerville |
NJ |
11/19/2009
|
| Truck Driver/Distribution Operator |
| A minimum of a High school diploma, G.E.D. or equivalent required. A minimum of a NJ state issued Class B Commercial Drivers License (CDL) is required. Experience operating a vehicle rated 26,000 lbs. or greater is required. A minimum of 3 year of experience driving a truck with CDL accreditation required. Experience in a warehousing operation environment preferred. Experience working in a Good Manufacturing Practice (GMP) or other regulated environment preferred. Basic math skills required. Basic computer skills required. Must have excellent communication and interpersonal skills. Must be detail-oriented and demonstrate alertness, accuracy and patience. Must follow good driving procedures and be highly safety conscious. Experience performing basic vehicle service is preferred. The ability to drive and handle a large panel truck on open highways and in congested areas required. The ability to operate a manual and motorized pallet/hand truck required. The ability to lift/carry up to 35 pounds unaided is required. The ability to work occasional overtime 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 |
Somerville |
NJ |
11/19/2009
|
| Regulatory Affairs Specialist |
| A minimum of a Bachelor's degree in Biology, Biochemistry, Immunology or a related discipline is required. A PhD degree in Biology, Biochemistry, Immunology or a related discipline is strongly preferred. A minimum of 2+ years experience in Regulatory Affairs required. Experience or exposure to the field of Biologics is required. Medical Device and Pharmaceutical experience is an asset. US Regulatory experience is required. EU and International Regulatory experience is an asset. Previous experience in regulations and submitting files for health authorities in Israel is an asset. Excellent communication skills will be necessary for this role. This position will require 10% travel and will be located in Somerville, NJ. |
| Johnson & Johnson Family of Companies |
Somerville |
NJ |
11/19/2009
|
| Manager, Regulatory Affairs |
| A minimum of Bachelor's degree in a technical, scientific, or medical/health discipline is required. An advanced degree is an asset. A minimum of 8+ years experience in a regulated healthcare industry is required. Direct experience in Regulatory Affairs is required. Experience with or exposure to 510(k) submissions is required. US regulations knowledge is required, with EU and International/OUS experience an asset. PMA experience is an asset. Copy review experience is an asset. RAC is an asset. Excellent verbal and written communication skills will be needed. The ability to influence and negotiate with business partners and regulatory agencies will be required. This position will be located in Somerville, 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! |
| Johnson & Johnson Family of Companies |
Somerville |
NJ |
11/19/2009
|
| Tool Room Technician |
| A minimum of a High school diploma, GED or equivalent required. Vocational, technical or apprenticeship training preferred. A minimum of 3 years of Millwright, HVAC, Pipefitter, Electrician and/or Machinist experience is required. Experience as a Mechanic in a commercial environment (i.e. manufacturing, industrial) is preferred. General maintenance experience preferred. Experience managing a tool crib or parts distribution preferred. Prior experience in a GMP, GLP ISO, QSR or other regulated industry is preferred. Must be a certified Forklift Operator or be willing to become certified. Must possess a current and valid driver's license. The ability to read and understand blueprints is preferred. Knowledge of Microsoft Office (Word, Excel, Outlook) preferred. Experience navigating in a Microsoft Windows environment required. Experience with Material Management software (i.e. CribMaster), Purchasing Systems (i.e. Ariba) and CMMS software (i.e. Maximo) preferred. Must have strong communication and interpersonal skills. Must be a team player and be able to work with minimal technical supervision. The ability to work occasional overtime, weekends and some holidays 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! |
| Astellas Pharma, Inc. |
Skokie |
IL |
11/19/2009
|
| Research & Development Future Opportunities |
| ? Positions in the Research & Development division at Astellas require degrees in science; advanced degrees plus industry experience are preferred. |
| 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. |
| Johnson & Johnson Family of Companies |
Skillman |
NJ |
11/19/2009
|
| MARKETING RESEARCH SUMMER INTERN |
| An applicant for this position should be a candidate for an MBA or MS in a Marketing Research program, with a strong academic record. The qualified candidate must be enrolled in an MBA or other business-related graduate program and planning to obtain your degree in or before July 2011. Other key qualities for success in these positions includes: The ability to think strategically and creatively. Exceptional communication and interpersonal skills. Results oriented with willingness to take responsibility and initiative. Excellent analytical skills and the ability to unbundle issues. The ability to be a team player. We have internship opportunities in Fort Washington, PA and Skillman, NJ locations. The candidate must be willing and able to intern in one of those locations. |
| Johnson & Johnson Family of Companies |
Skillman |
NJ |
11/19/2009
|
| 2010 MBA Marketing Summer Intern, NJ |
| 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 work in one of the following locations: Skillman NJ or Morris Plains, NJ. |
| International Partnership for Microbicides, Inc. |
Silver Spring |
MD |
11/20/2009
|
| Executive Assistant |
| â?¢ Associate/Bachelorâ??s degree or equivalent experience working in position with similar responsibilities.
â?¢ Minimum five years administrative experience assisting senior level executives with demonstrated experience in positions that require maturity, poise, ability to handle sensitive information and communicate with high level stakeholder and constituents.
General office in downtown Silver Spring, Maryland. Job holder should expect fast-paced, dynamic working environment.IPM is an Equal Employment Opportunity Employer. |
| 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. |
| 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 |
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! |
| Agilent Technologies, Inc. US |
Schaumburg |
IL |
11/20/2009
|
| Service Technical Specialist |
| Requires higher education or specialized training/certification.
Requires a minimum of 5 years directly related calibration/repair experience, with typically 7 to 10 years experience. Expert skills in the calibration and repair of all types of Agilent and Multivendor Test Equipment. Experience using automated calibration software platforms (STE, PC Based, Metcal, TME etc) required.
Requires excellent communication and organizational skills. |
| Agilent Technologies, Inc. US |
Santa Rosa |
CA |
11/20/2009
|
| R&D Engineer, Software |
| ? University degree in Electrical Engineering (MS level) required, PhD. in the EM simulation area highly preferred.
? Thorough understanding of EM simulation techniques, particularly in time domain methods, as well as their software implementation aspects, including the implementation of complex numerical algorithms.
? Good understanding on the application areas of EM simulation products.
? Experience in numerical/scientific programming in C/C++ and generally good software development skills
? The ability to work in a multi-site, multi-cultural team environment |
| Agilent Technologies, Inc. US |
Santa Rosa |
CA |
11/20/2009
|
| Semiconductor Fab Integration Engineer |
| M.S. or Ph.D. in Electrical Engineering, Physics, Materials Science, Mechanical Engineering, Chemical Engineering or equivalent experience.
Experience with advanced semiconductor and/or MEMS processes and devices is essential and specific skills in III-V device physics and processing are highly desirable.
Experience with statistical process control and design of experiments is desired.
Candidates should have excellent interpersonal, problem solving, and communication skills for successful inter-group and intra-group interactions.
US Citizenship/Permanent Resident status is recommended, but applications from highly qualified candidates requiring work sponsorship will also be considered.
Candidates requiring work sponsorship must be eligible for access to export controlled electronics technology.
Geo Location: Santa Rosa, CA
~cb~11/02/09 |
| Agilent Technologies, Inc. US |
Santa Rosa |
CA |
11/20/2009
|
| Productivity Engineer |
| Musts
- 5 years minimum experience in PCB layout
- 3 years minimum experience in high-speed digital and/or high-frequency RF PCB layout
- Expertise with Mentor Graphics Expedition and specifically Expedition CES
- Expertise in manufacturing output processes, data, and tools
- Experience with Mentor BoardStation layout
- Excellent troubleshooting skills and ability to trace problems to root cause in layout
- Knowledge and familiarity with PCB fabrication and assembly technologies and processes
- Experience with the Valor design rule checker
- AS degree in electronics, Computer-Aided drafting, or equivalent
- Excellent communication skills and ability to do multitasking
- Good computer skills
Wants
Skill or experience in the following areas would be a plus, but aren't required.
- Programming skills in scripting (e.g., VBscript, Perl, Javascript)
- Documentation and technical writing skills
- Familiarity with component library and schematic tools
- Electronic circuit design experience
- Familiarity with other PCB tools besides Mentor Graphics (e.g., Cadence, Zuken, Intercept) and can objectively evaluate and recommend best tools and practices
- Experience in systems and EDA tool administration
- Bachelors degree in electrical engineering or equivalent
~cb~11/17/09 |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
11/19/2009
|
| Research Associate/Senior Research Associate: Target validation and Protein Expression |
| The position requires a BS or MS in Biology or a related field with a minimum 2 years of practical experience in a research laboratory. Industry or academic experience and previous work in biochemical, cancer, immunological, cell culture and molecular biology techniques are essential. Excellent verbal and communication skills, and the ability to work both independently and in a team environment are required. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
11/19/2009
|
| Scientist, Target Discovery -- Agensys, Santa Monica, CA |
| The successful candidate will have a PhD in molecular biology, biotechnology, biochemistry or related discipline with minimum 5 years of relevant industry experience. Other required experience includes expertise in a broad range of molecular and cellular techniques surrounding aspects of microarray-based discovery, biomarker identification and target selection for product development. Experience with management of research associates and demonstrated leadership is preferred. Excellent verbal and communication skills, as well as the ability to work in a dynamic team environment are essential. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
11/19/2009
|
| Scientist/Sr Scientist, Translational Research -- Agensys, Santa Monica, CA |
| Candidate consideration requires a Ph.D. in molecular and cellular biology or similar field with a minimum of 6 years of post-doctoral experience. Industrial experience in Oncology drug discovery and experience managing research associates is highly preferred. Successful candidates will have strong written and oral communication skills, be self-motivated, demonstrate leadership and possess an exemplary record of research, as evidenced by publications and patents. Developmental opportunities include leading projects for therapeutic antibody discovery, building new technology platforms, and team leadership. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
11/19/2009
|
| Senior Research Associate, In vivo validation - Agensys - Santa Monica, CA |
| The ideal candidate should have a MS in biological sciences with a minimum of 5 years experience in biological research, preferably in an industry setting. Previous experience in handling research rodents, especially immunodeficient mice, is absolutely required. Experiences in pre-clinical validation of cancer therapeutics using xenograft models, performing microsurgical procedures in rodents, xenograft tumor characterization and mammalian cell culture are highly desired. We are seeking a flexible, enthusiastic individual with good organizational and communication skills and the desire to work in a dynamic team environment. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
11/19/2009
|
| Manufacturing Associate (temp to perm), Agensys, Santa Monica, CA |
| Clinical or commercial manufacturing experience preferred. Broad based technical knowledge with manufacturing equipment (i.e. Bioreactors, filtration, mixers, purification etc.). Excellent organizational skills, written and oral communication skills and ability to multi-task. Must possess mechanical aptitude |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
11/19/2009
|
| Manufacturing Associate II-- Agensys, Santa Monica, CA |
| BS in biological or other science related field and 3+ years relevant industrial experience in the manufacture or development of FDA regulated Biological Products. Clinical or commercial manufacturing experience preferred. Broad based technical knowledge with manufacturing equipment (i.e. Bioreactors, filtration, mixers, purification etc.). Excellent organizational skills, written and oral communication skills and ability to multi-task. Must possess mechanical aptitude. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
11/19/2009
|
| Sr. Scientist/Scientist - Preclinical Bio-Imaging, Agensys - Santa Monica, CA |
| ? PhD with a background in radiology, cancer or cell biology that includes analyzing and interpreting imaging data? Minimum of 4-5 years of industrial or academic experience in relevant fields? Research experience in small animal imaging, managing relevant equipment and interpreting radiopharmaceutical experiments is critical? Experience with use of in vivo models to explore PK, PD and efficacy and their relationship with biomarker expression is highly desirable ? A proven publication record is desirable? Ability to take charge and drive projects to completion? Effective interpersonal and technical communication skills with ability to report and communicate study outcomes to project team(s)? Ability to work in a team oriented environment and oversee portions of studies performed by other groups or departments? Understanding of ALAAC accreditation and IACUC protocols is highly desirable. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
11/19/2009
|
| Senior Scientist/Scientist, Cell Line Development - Agensys, Santa Monica, CA |
| The successful candidate will have a PhD in biotechnology, cell biology, biochemistry or related discipline with minimum 5 years of relevant industry experience. Other required experience includes expertise in a broad range of molecular and cellular techniques surrounding aspects of cell culture, vector development and expression technologies, cell line development, and cell banking. Experience with management of research associates and demonstrated leadership is preferred. Excellent verbal and communication skills, as well as the ability to work in a team environment are essential. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
11/19/2009
|
| Research Associate, Translational Research - Agensys, Santa Monica, CA |
| Candidate consideration requires a BS/MS in molecular and cellular biology or similar field with a minimum of 3 years of relevant laboratory experience. Industrial experience in Oncology drug discovery is preferred. Successful candidates will have strong written and oral communication skills and be self-motivated. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
11/19/2009
|
| Research Associate/Senior Research Associate: Target function ? MAb assays - Agensys, Santa Monica, CA |
| The position requires a BS or MS in Biology or a related field with a minimum 3 years of practical experience in a research laboratory in the required activities. Industry experience and previous work in biochemical, immunological, cell culture and cell-based techniques are essential. Excellent verbal and communication skills, and the ability to work both independently and in a team environment are required. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
11/19/2009
|
| Sr. Administrative Assistant- Agensys, Santa Monica, CA |
| A minimun of 5 years administrative assistant experience including general office coordination responsiblities.A college degree and previous expereince at a biotech, pharmaceutical or healthcare company highly preferred.Strong expertise with Microsoft Office, Oracle and telephone protocol required. Duties require professional verbal and written communication skills and the ability to type 60 wpm. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
11/19/2009
|
| Facilities Department Planner/Assistant |
| ? An Associates of Arts degree preferred? A minimum of two years experience working in an FDA regulated environment? A working knowledge of Computerized Maintenance Management Systems? Self-starter with the ability to work with minimum supervision? Excellent verbal and written communication skills? The ability to multitask and exercise good judgment? The ability to work in a fast pace environment and maintain a high level of customer service? Detailed oriented with good follow-up skills? Proficient in computer usage with standard business software |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
11/19/2009
|
| Associate Director/Director, Toxicology- Agensys, Santa Monica, CA |
| ? Ph.D in toxicology, biochemistry, pharmacology, pharmacokinetics or related sciences; minimum of 10 years of pharmaceutical industry, including 7 years in toxicology and management experience ? Comprehensive knowledge of drug development (non-clinical and clinical) ? Experience with non-clinical CROs ? Knowledge and experience in biopharmaceutics, toxicology, toxicokinetics, ADME and pharmacokinetics with therapeutic antibodies and antibody drug conjugates ? Knowledge of FDA regulations pertaining to non-clinical and clinical drug development. ? Well developed oral and written communication |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
11/19/2009
|
| Cell Culture Engineer/Associate, Agensys, Santa Monica, CA |
| ? A B.S. or M.S. in biochemistry, biology, biochemical engineering or a related field. ? 1 to 3 years related experience in the biopharmaceutical/biotech industrial ? Prior hands-on experiences in cell culture process development, especially with shake flasks and bioreactors.? Possess good problem solving, organizational, and documentation skills with a strong focus on details? Must have excellent organizational and communication skills? Must be highly motivated, be able to work independently as well as in teams |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
11/19/2009
|
| Cell Line Development Research Associate ? TEMP Position --Agensys, Santa Monica, CA |
| The ideal candidate will have a M.S. or B.S. in Cell Biology or related field, with a minimum of three (3) years of relevant experience. Experience in antibody expression systems, production cell line generation, and antibody characterization is preferred. Excellent verbal and communication skills, as well as the ability to work in a team environment are essential. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
11/19/2009
|
| Director, Regulatory Affairs- Agensys, Santa Monica, CA |
| Bachelor?s degree in life sciences, Chemistry, Biology preferred. Advanced degree is a plus. 8-10 years previous biotechnology and/or pharmaceutical drug development experience. Scientific knowledge in chemistry, general biological/physical science and ability to apply that knowledge to regulatory issues and product development. Recognized as an expert in regulatory strategy and submissions. A minimum of 5 years regulatory affairs experience preferably involving direct contact with the FDA; full knowledge of FDA & ICH regulations and guidelines, and the ability to provide interpretations of that information to others. Proven record of successful IND/NDA submission and negotiations with the FDA. Strong organizational skills with the ability to manage large projects and provide regulatory guidance/training to others in the department as needed. Proven ability to prioritize and multi-task with minimal supervision based on interactions with project team members. Excellent written and oral communication skills, with writing ability to meet regulatory requirements and standards. Ability to communicate effectively and maintain effective working relationships. Must be able to positively influence direct Agensys staff and colleagues and groups within Astellas global organization. Highest integrity with respect to professional standards and maintenance of proprietary, confidential information. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
11/19/2009
|
| Director/Senior Director, Molecular Discovery -- Agensys, Santa Monica, CA |
| ?X Advanced degree (Ph.D., or equivalent) with at least 10 years experience in an industry setting, molecular biology, molecular genomics, bioinformatics and related areas. with demonstrated track record of ?X Proven record in design and implementation of activities related to gene discovery and characterization, gene profiling, bioinformatics, ?X Demonstrated record in driving scientific and technical innovations, as evidenced by first or senior authored publications in top-tiered journals?X Demonstrated successful program leadership and multi-project coordination ?X At least 5 years of management experience of multiple groups ?X Proven track record in leading programs to achieve goals and timelines?X Ability to perform successfully in a cross-functional team environment?X Excellent written and verbal communication skills |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
11/19/2009
|
| Formulation Development Scientist -- Agensys, Santa Monica, CA |
| ? Ph.D. in a scientific discipline (Biochemistry, Chemical Engineering, or Biochemical Engineering) with 5+ years of relevant experience in the pharmaceutical /biotechnology industries.? Experience in the pharmaceutical industry is preferred in formulation development or related biochemistry related areas of development (e.g. purification, stability, analytical). ? Experience working with monoclonal antibodies and exposure to early phase formulation development activities? Experience with IV formulations as well as formulation development for poorly soluble compounds would be desirable. ? Proven experience managing the scale-up and manufacturing of parenteral dosage forms? Proven ability to apply the principles of the basic sciences, such as physical and organic chemistry, thermodynamics, and materials science, to pre-formulation and formulation development, using a rational, scientific approach.? Supervisory experience preferred. ? Must be highly motivated, have excellent organizational and communication skills, and must be able to work independently and as part of a multi-disciplinary team. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
11/19/2009
|
| Research Associate ? Antibody Production, Hybridoma, Agensys - Santa Monica, CA |
| ?X BSc or MSc in Cellular Biology, Biology, Bioprocess Engineering or related field. ?X Minimum of 2 years relevant experience. ?X Extensive mammalian tissue culture experience, preferably gained in an antibody production environment. ?X Knowledge of antibody production from hybridoma or recombinant cells. ?X Excellent verbal and written communication.?X Excellent organizational skills.Additional skills (useful but not essential):?X Experience with wave form bioreactors?X Experience with stirred tank bioreactors |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
11/19/2009
|
| Research Associate Antibody Production, Agensys - Santa Monica, CA |
| ?X Bachelors, or Masters Degree in Cellular Biology, Bioengineering, Microbiology or a related field. ?X Minimum of 2 years post graduate experience. ?X Extensive mammalian tissue culture experience, preferably gained in an antibody production environment. ?X Knowledge of process development for antibody production from hybridomas or recombinant cells; experience with techniques to improve recombinant protein expression by stable mammalian cell lines is advantageous?X Applicants should be well organized, self-motivated, and capable of working independently and in a collaborative environment. ?X Experience in antibody purification techniques is desirable but not essential as full training will be given.?X Excellent verbal and written communication?X Excellent organizational skills. ?X Meticulous note keeping will be essential |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
11/19/2009
|
| Research Associate, Target Validation and Protein Expression, Agensys - Santa Monica, CA |
| The position requires a BS or MS in Biology or a related field with a minimum 2 years of practical experience in a research laboratory. Industry or academic experience and previous work in biochemical, cancer, immunological, cell culture and molecular biology techniques are essential. Excellent verbal and communication skills, and the ability to work both independently and in a team environment are required. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
11/19/2009
|
| Research Associate, Cell Line Development - Agensys, Santa Monica, CA |
| The ideal candidate will have a M.S. or B.S. in Molecular Biology or related field, with preferably a minimum of three (3) years of relevant experience in industry. Experience in antibody expression systems, production cell line generation, and antibody characterization is required. Excellent verbal and communication skills, as well as the ability to work in a team environment are essential. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
11/19/2009
|
| Research Associate, Target Discovery -- Agensys, Santa Monica, CA |
| The ideal candidate will have a M.S. or B.S. in Molecular Biology or related field, with preferably a minimum of three (3) years of relevant experience in industry. Experience in microarray systems, data analysis, RNA isolation, and real-time PCR is required. Excellent verbal and communication skills, as well as the ability to work in a team environment are essential. |
| Astellas Pharma, Inc. |
Santa Monica |
CA |
11/19/2009
|
| Research Associate, Target Validation and Protein Expression, Agensys - Santa Monica, CA |
| The position requires a BS or MS in Biology or a related field with a minimum 2 years of practical experience in a research laboratory. Industry or academic experience and previous work in biochemical, cancer, immunological, cell culture and molecular biology techniques are essential. Excellent verbal and communication skills, and the ability to work both independently and in a team environment are required. |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
11/20/2009
|
| LC/MS Proteomics Scientist |
| PhD Degree or equivalent in Chemistry, BioChemistry, Biology, or related field.
Minimum of 4 years relevant experience.
The successful person for this position will:
? Be comfortable with all aspects of LC/MS analysis of proteins: sample preparation, instrument operation, data analysis, and data interpretation and processing
? Have the ability to use mathematical, theoretical modeling and software tools to develop predictive models for improving methods and data mining algorithms
? Have an understanding of the use of statistics in data interpretation and experimental design
? Be well-versed in the scientific method
? Have an understanding of mass spectrometry instrumentation, ion optics, and sources
? Have familiarity with and the ability to write software tools to assist in data mining
? Have a good understanding of proteomics in relation to other aspects of systems biology
? Be an effective communicator and team player
~cb~11/12/09 |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
11/20/2009
|
| Applications Engineer |
| Requires:
- BS in biology, biochemistry, molecular biology; related discipline or equivalent. Master or PhD preferred.
- 3+ years experience with life science software products
- Experience with systems biology software products
- Experience in interacting with customers in a pre-sales and/or post sales support role
- Experience in generating and presenting technical training materials
- Experience in interacting with cross-functional groups including sales, marketing and R&D
Geo Location: Santa Clara, California
cb~09/11/09 |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
11/20/2009
|
| Nucleic Acid Chemist - Genomics R&D |
| Qualifications :
? Ph.D. degree in Organic Chemistry, Biochemistry or equivalent
? 4+ years relevant experience in industry and/or academia
? Strong theoretical knowledge and hands-on applications of modern Nucleic Acid chemistries required
? Strong knowledge and experience developing DNA and RNA synthesis processes is highly desired
? Knowledge of Chemical and Physical property Analytical techniques is highly desired, including LC/MS, NMR, viscosimetry, tensiometry, etc.
? Knowledge of Surface chemistry and surface analytical techniques a plus
? Proficiency in molecular biology techniques (electrophoresis, enzymatic assays, ?) and experimental troubleshooting a plus
? Proficiency with PCR & qPCR methodologies a plus
? Previous experience with microarrays and a working knowledge of statistical methods a plus
? Computer literacy and hands-on experience working with database software applications
? Excellent communications skills and time management skills
? Ability and enthusiasm to work in a collaborative team environment
~cb~11/12/09 |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
11/20/2009
|
| R&D Bioinformatics, Software Engineer |
| External Qualifications:
This dynamic position requires a MS degree in Computer Science or equivalent plus a minimum of 5+ years relevant experience with bioinformatics tools and procedures as applied to high-throughput computational pipelines.
Chosen candidate must have the following:
? 5+ years experience in C++, .NET, and Java
? Object oriented programming experience a plus
? Experience with: BLAST, BLAT and/or MOST
? Experience with SQL and/or Oracle database
? Knowledge of public biological databases, tools, and repositories is required
? Hands-on experience producing software in collaborative, multidisciplinary environment to solve problems in biological or other life science is highly desirable
? Experience with Image Analysis is a plus
Geographic Location: Bay Area, California (Santa Clara)
~cb~10/19/09 |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
11/20/2009
|
| Human Resources Business Partner |
| ? BS/MS Degree in Business/ HR/OD or equivalent
? 8 years business experience in progressively challenging responsibilities in the following areas: leadership development of senior business team, organizational development/effectiveness, consulting, change management and talent management.
? A minimum of 3-5 years of HR experience within the Life Sciences space.
? Experience supporting Life Sciences channels preferred.
? A working knowledge of general HR practices a must along with the ability to influence HR strategy and policy using previous knowledge and experience from other business and work environments.
? The successful candidate will be an experienced business and human resources professional who has had experience within a heavily matrixed organization. This candidate will have related industry experience in the life science/biotech industry, with an emphasis in strategic planning, the ability to facilitate and relate to people across cultures and levels, and proven leadership skills.
Geo Location: San Francisco/Bay Area |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
11/20/2009
|
| Applications Scientist - Microarrays & QPCR |
| Key Areas of Expertise:
Must have expertise in the following key areas:
-Microarrays ? Agilent arrays: Gene Expression, ChIP-on Chip, CGH
-QPCR ? both probe and SYBR Green assay experience desired
-Agilent Bioanalyzer
-Use of bioinformatics software, such as GeneSpring or ArrayAssist to analyze microarray data
Education/Experience:
?Must have a B.S. or M.S. in Biology, Molecular Biology, or Biochemistry. A PhD is preferred.
?5 years lab experience with microarrays and QPCR
?Lab experience with Stratagene and Agilent products is a plus
?Must be a team player
?Excellent verbal and written communication, organizational, and project management skills
-Ability to interface with global multidiscipline internal/external cross function teams
-Ability to demonstrate excellent outbound phone calling communication skills.
-Ability to solve a broad range of problems of varying scope and complexity.
-Proactively acts to understand customer needs and identify solutions to non-standard tasks/queries; actively creates business opportunities.
Geo Location: May reside in the Santa Clara, CA - La Jolla, CA - or Wilmington De Office
No relocation assistance available.
cb~10/08/09 |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
11/20/2009
|
| Product Marketing Engineer |
| ? Bachelor of Science in biology, biochemistry, molecular biology, bioinformatics, or related discipline is required. Master or PhD preferred.
? Ability to communicate and discuss technical information on copy number and SNP analysis/bioinformatics, genetics, and genomic studies.
? Knowledge of key software platforms for genetic analysis and bioinformatics tools and databases such as the eArray, DGV, NCBI and UCSC Genome Browser.
? Exceptional cross-functional communication skills - proven ability to influence at all levels of the organization.
? Demonstrated use of marketing skills and market knowledge to define and commercialize products that result in business success.
? Experience in working with worldwide customers and is a strong advocate for customer focus and customer driven development. |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
11/20/2009
|
| Senior Software Engineer |
| Job requirements:
? Demonstrated C/C++ programming skills in a product-development environment.
? Demonstrated knowledge of STL, MFC, ATL, ActiveX, and other related software technologies.
? Experience with Microsoft Visual Studio and other software-development tools required.
? Experience investigating newer technologies and evaluating feasibility of utilizing newer technologies for system platforms.
? Experience synthesizing a cohesive system consisting of hardware, electronics, firmware, and software.
? Ability to work collaboratively in team environments.
? Ability to provide clear and concise oral and written communication of product concepts and engineering requirements.
? Ability to follow both written and verbal directions and ask questions when necessary.
? Ability to adhere to a quality control system.
? Willingness to exercise considerable independent judgment.
? Demonstrated strong follow-through with thorough attention to detail.
Education/Experience:
? Bachelor's degree in computer science, engineering, or related field. Advanced degrees are strongly preferred.
? 10+ years of technical experience required, with past work on product-development teams strongly preferred.
? Experience developing production-quality software required, with robotics and automation experience a plus.
~cb~10/29/09 |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
11/20/2009
|
| Software Engineer |
| Educated to at least university degree level, you'll also have 5+ years' practical R&D experience, including at least 3 years' in a similar environment. A keen problem-solver with a proactive, team-oriented approach, you'll relish the challenges this pioneering environment presents.
~cb~10/29/09 |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
11/20/2009
|
| Software Engineer |
| Educated to at least university degree level, you'll also have 5+ years' practical R&D experience, including at least 3 years' in a similar environment. A keen problem-solver with a proactive, team-oriented approach, you'll relish the challenges this pioneering environment presents.
~cb~10/29/09 |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
11/20/2009
|
| LC/MS Research |
| Required qualifications:
? Recent Ph.D. degree in chemical or biological sciences
? Familiarity with HPLC/MS technologies.
? Demonstrated proficiency in laboratory research.
? Ability to quickly learn and develop new laboratory skills and techniques.
? Preference to work within a multidisciplinary team and with leading edge external collaborators.
The following additional skills are highly desired:
? Experience in nanoLC/MS and its applications.
? Proficiency using high level programming languages for data acquisition, analysis and instrumentation control.
? Exceptional skills in quantitative data analysis.
? Excellent communication skills.
~cb~10/26/09 |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
11/20/2009
|
| SAP Technical Lead, Expert |
| ? Proven ability to develop plans and lead technical teams in the delivery of IT projects and services.
? Demonstrated knowledge and proficiency of the Basis aspects of complex SAP environments and integration with other platforms and technologies.
? Demonstrated ability to manage large IT/business projects and programs through all phases of the project life cycle, including 3rd party resources.
? Participated in two or more full project life cycle implementations of various SAP modules.
? Demonstrated skills and proficiency of the SAP Netweaver environment with SAP ECC, CRM, APO, and BI.
? High level of understanding of eSOA and enterprise portal.
? Extensive hands on exposure to SAP environment planning, monitoring, and optimization tools.
? Excellent written and verbal communication skills in English; ability to present complex information in a clear and structured way; ability to work at all levels in the organization (end users to executives, IT and business).
? Bachelors Degree in Information Systems or Computer Science, with a focus on business applications and Information Technology. Advanced degree is preferred. Minimum of 10 years in an SAP environment, including 5+ years of technical team lead experience.
~cb~10/23/09 |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
11/20/2009
|
| Applications Engineer |
| Requires:
- BS in biology, biochemistry, molecular biology; related discipline or equivalent. Master or PhD preferred.
- 3+ years experience with life science software products
- Experience with systems biology software products
- Experience in interacting with customers in a pre-sales and/or post sales support role
- Experience in generating and presenting technical training materials
- Experience in interacting with cross-functional groups including sales, marketing and R&D
Geo Location: Santa Clara, California |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
11/20/2009
|
| HPLC Bio-Separations Application Chemist |
| ? Advanced Degree in Biochemistry, Molecular and Cellular Biology, or equivalent (demonstrated by 5+ years working experience in analytical HPLC bio-separations and confirmation of technical HPLC and Bio-Chromatography knowledge)
? Demonstrated expertise in operating HPLC systems and using a variety HPLC Bio-Columns including ion exchange, size exclusion, reverse phase, hydrophobic interaction and affinity
? Demonstrated experience in operating LC/MS and/or capillary electrophoresis systems for Biologic analysis preferred but not required
? Proven track record of self motivation and initiative
? Excellent verbal and written communication skills
? Ability to travel world wide as required up to 30% of the time
? Biopharmaceutical or Biotechnology expertise is critical to this position
~cb~11/01/09 |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
11/20/2009
|
| Regional Government Security Manager (West) |
| - MUST currently hold a SCI level security clearance with a current Single Scope Background Investigation (SSBI).
- Must have a firm understanding of the security policies, procedures and directive of the DoD, National Industrial Security Program and Intelligence Community SCI security programs.
- Bachelors Degree in Criminal Justice, Security Management, Industrial Security, Business Management or equivalent combination of education and experience.
- 5 to 10 years of experience in the Government Security Field.
- Knowledgeable in the use of JPAS, DIAS COMSEC and DoD/OPM Electronic Personnel Security Questionnaire software packages.
- Proficiency with Microsoft Office products is essential.
- Requires the ability to make sound decisions, manage time, take independent action, analyze problems and provide focused solutions.
- Demonstrated ability to effectively communicate information to various audiences and all levels of the organization both verbally and through written communications.
- Must be highly organized, be willing to work in a team environment, be able to prioritize tasking, perform in a multi-tasked and dynamic environment.
- Must be dependable, responsive, customer focused and possess the qualities of diplomacy, tact, excellent judgment, discretion and initiative.
~cb~10/05/09 |
| Agilent Technologies, Inc. US |
Santa Clara |
CA |
11/20/2009
|
| NPI Engineering - Mass Spectrometer Instrumentation |
| Requires:
- BS/MS degree in Electrical Engineering or equivalent
- 2+ yrs industry experience working on the NPI of large integrated systems
- Experience in bringing new product design from R&D to scalable manufacturing
- NPI experience of Mass Spectrometer Instrument Systems highly desired
- knowledge of electrical theory, components, and circuits
- Experience with high voltage components desired
- Knowledge of PCA test methods
- Excellent written and verbal communication skills
- Track record of success working within cross functional /cross regional teams
- DFX Experience
- Available for up to 10% business travel
Geo Location: Santa Clara, CA
~cb~8/17/2009 |
| Astellas Pharma, Inc. |
Santa Barbara (1P060410) |
CA |
11/19/2009
|
| Professional Representative, PCP - Santa Barbara, CA |
| THE SUCCESSFUL CANIDATE FOR THIS ROLE WILL HAVE:- A Bachelor Degree- Excellent communication, facilitation and presentation skills- Can do approach and very high motivational and persuasion skills- Some experience (1 year) with business-to-business sales If you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you. |
| Johnson & Johnson Family of Companies |
Santa Barbara |
CA |
11/19/2009
|
| Associate Director, Business Analytics (Mentor Corporation Santa Barbara, California) |
| BS or BA required. Concentration business, marketing, finance, statistics, mathematics, or related field preferred. Advanced degree or MBA preferred. A minimum of 8 years of progressive experience in forecasting, business analytics, finance, market research, portfolio analysis, or a related field is required. Experience in the medical device, hospital specialty, or healthcare field is preferred. A minimum of 3 years experience managing people required. Proficiency in Microsoft EXCEL, PowerPoint, Crystal Ball, or Risk is required. Excellent leadership, collaboration, communication and analytical skills are required. Must be able to influence and impact others through building and defending arguments and reaching consensus of opinion. Excellent verbal and written presentation skills are required. Must be able to understand and translate data into actionable insights to support decision-making. Must be results-driven with ability to lead a team and create a productive environment for employees to consistently maintain high performing standards. Strong listening and project planning skills are required. Experience in creating market models and revenue forecasts is required. Deep knowledge of qualitative and quantitative marketing research methodologies and related statistics required. Working knowledge of industry primary, secondary data and competitive intelligence data is strongly preferred. Demonstrated success in creative problem solving and team partnership is required. This position is based in Santa Barbara and requires 30% travel as needed. |
| 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 |
| 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 |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Scientist I |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Research Associate |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Accounting Manager |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Bioprocess Engineer I |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Bioprocess Engineer I |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Bioprocess Engineer I |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| EBusiness Applications Manager |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Director of Campaigns |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Clinical Data Analyst |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Bioprocess Engineer II |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Bioprocess Engineer II |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Manager International Regulatory Affairs |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Instrument Assembly Associate I |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Sr Scientist |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Sr Reagent Dev Associate |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Sr Algorithm Scientist Developer |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Software Project Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Software Project Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Manager US Regulatory Affairs |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| New Product Launch Coordinator |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Reagent Dev Associate III |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Reagent Dev Associate III |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| WW Controller Cell Analysis |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Production Chemist I |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Project Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Program Manager |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Production Technician II |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Production Technician I |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Project Manager, IT |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| QA Technician II -FPR |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Quality Engineer II |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Quality Engineer II |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Sr. Manufacturing Equipment Engineer - Reagents |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Reliability Engineer II |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Senior Intellectual Property Counsel |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Technical Support: Technical and Informatics Support Specialists (TAISS) |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Technical Applications Specialist |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Technical Writer IV |
| See above |
| Johnson & Johnson Family of Companies |
San Francisco |
CA |
11/19/2009
|
| Senior Database Administrator (Contract) |
| A minimum of 3 years of experience as MySQL DBA on Unix/Linux on MySQL 4.1 and/or 5.0. Excellent knowledge and experience in InnoDB & MyISAM is required. Experience in DB backup, recovery, replication, High Availability is required. Experience as an Oracle DBA (RMAN, standby server) is nice to have. Excellent skills in SQL and scripting languages (Perl/Python/Unix Shells, etc.) is desired. Nagios or Cacti monitoring work is a plus. This role will require 24/7 pager rotation. |
| Johnson & Johnson Family of Companies |
San Francisco |
CA |
11/19/2009
|
| San Francisco/Sacramento, CA: 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 |
San Francisco |
CA |
11/19/2009
|
| Digital Interactive Marketing Manager (Contract) |
| A minimum of 3 years of interactive marketing, sales, or agency experience is required. Specific focus in building rapid, yet comprehensive and polished custom client presentations is required. A strong understanding of basic marketing principles and how to use qualitative and quantitative information to develop successful solutions and pitches is required. Ability to prioritize and manage multiple projects in busy environment is required. Excellent oral and written communication skills are required. Strong presentation building skills is required. High degree of proficiency in Microsoft Office (Excel, Word, PowerPoint) and Photoshop is required. Must be able to thrive in a fast-paced work environment. Must be a strong team player with a can-do, pitch in attitude. Must be capable of working proactively with multiple departments to achieve results. Agency experience is preferred. |
| BD (Becton, Dickinson and Company) |
San Diego |
CA |
11/20/2009
|
| Scientist I |
| See above |
| BD (Becton, Dickinson and Company) |
San Diego |
CA |
11/20/2009
|
| Scientist I |
| See above |
| BD (Becton, Dickinson and Company) |
San Diego |
CA |
11/20/2009
|
| Research Associate III |
| See above |
| BD (Becton, Dickinson and Company) |
San Diego |
CA |
11/20/2009
|
| Marketing Manager |
| See above |
| BD (Becton, Dickinson and Company) |
San Diego |
CA |
11/20/2009
|
| Biochemist I |
| See above |
| Agilent Technologies, Inc. US |
San Diego |
CA |
11/20/2009
|
| Field Service Technician |
| Qualifications: Associates Degree in Electronics or recent Military experience/training in electronic measurement calibration and a minimum of 2 years field experience.
Position requires:
? Hands-on Experience as Field Service Engineer or Maintenance Technician
? Knowledge of the calibration and repair of all types of electronic equipment
? Excellent communication skills (customer interface skills)
? Strong organizational skills
? Positive/Energetic attitude
? Willingness to learn |
| BD (Becton, Dickinson and Company) |
San Diego |
CA |
11/20/2009
|
| Instrumentation Technician I |
| See above |
| BD (Becton, Dickinson and Company) |
San Diego |
CA |
11/20/2009
|
| Manufacturing Manager - Tissue Culture |
| See above |
| Vertex Pharmaceuticals |
San Diego |
CA |
11/19/2009
|
| Intern - Instrumentation |
| Must be a current student enrolled in Electrical Engineering. This is a paid internship.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
San Diego |
CA |
11/19/2009
|
| Senior Engineer |
| Job Requirements:
* Minimum of a Bachelor?s degree or equivalent in Computer Science, Information Systems, Engineering, or related technical discipline (required) Minimum 3+ years experience as a network administrator in Foundry or Cisco environment
* General network builds and administration
* Experience with industry standard network analysis and management tools.
* Configuring network switches and routers
* Experience managing dedicated appliances (Juniper VPN, Cisco Wireless, RSA)
* Experience with configuring Foundry equipment (switches, routers, etc?).
* Experience in LAN/WAN/Security network architecture development and associated financial analysis.
* 5+ years of Linux systems administration
* Perform day-to-day administrative support for Linux (CentOS, Redhat) environments
* Install Configure & Deploy Linux servers.
* Maintenance of local H/W and S/W configurations
* Experience with data protection software (e.g. CommVault)
* 5+ years experience in a 200+ server environment
* RedHat Linux 3.x through 5.x
* Strong Scripting (Perl, Shell, etc) abilities
* Citrix experience a plus
* Oracle experience a plus
* VMWare experience a plus
* Excellent communication skills both written and verbal
* Strong organization and problem solving skills, as well as a willingness to work cross-functionally with other teams in the organization.
* Research, Pharmaceutical & FDA regulated experience a plus
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
San Diego |
CA |
11/19/2009
|
| Scientist I (Analytical Development) |
| · Requires a PhD degree in Chemistry and 1+ years of relevant experience; or MS degree in Chemistry and 3+ years of relevant experience; or a BS degree in Chemistry and 6+ years of relevant experience.
· Must have a natural products, analytical chemistry or synthetic organic chemistry background.
· Strong knowledge of modern analytical chemistry techniques including separation techniques and mass spectrometry experience is required.
· Familiarity with Agilent and Thermo Mass spectrometry instrumentation and software is desirable.
· Previous pharmaceutical industry experience would be preferred.
· Must be highly self-motivated, highly productive with strong problem solving skills and be capable of working both independently and in a collaborative interdepartmental setting.
· Strong written and verbal communication as well as interpersonal skills are a must.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
San Diego |
CA |
11/19/2009
|
| Temporary Scientific Associate (Analytical Development) |
| * Requires a BS degree in Chemistry and 5+ years of relevant experience or MS degree in Chemistry and 3+ years of relevant experience.
* Must have analytical chemistry experience in a pharmaceutical or related field.
* Must have experience using HPLC/GR instruments.
* Chemical Manufacturing & Control (CMC) environment experience is highly preferred.
* Highly self-motivated, you must have good communication skills both written and verbal, be able to multitask, be flexible and have the ability to work in a flexible cross-functional team environment.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
San Diego |
CA |
11/19/2009
|
| Temporary ContractsParalegal |
| Qualified candidates must have a minimum of 1 ? 3 years corporate law experience or larger firm working primarily in contracts, paralegal certification preferred. Must possess high attention to detail, strong work ethic, be able to take initiative, and have excellent time management and follow-through skills. Must also demonstrate solid written and oral communication skills. Paralegal Certificate and BS or higher required (in a science field preferred). Experience with research & development contracts is a plus.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
San Diego |
CA |
11/19/2009
|
| Temporary Research Assistant (Compound Transfer Project) |
| High School diploma, AA or AS and some experience preferred
* Previous lab experience is a plus
* High level of attention to detail
* Well organized and conscientious
* Ability to remain focused while doing repetitive tasks with minimal supervision
* Basic PC and data entry skills
* Must be able to work Monday thru Friday, 40 hours per week and make a 3 month commitment.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
San Diego |
CA |
11/19/2009
|
| Temporary Research Associate (Cell Core) |
| We are seeking an associate with at least one year of cell culture experience and a BS degree. The successful candidate needs to be detail orientated while also having experience dealing with multiple cell lines at one time. Must have experience freezing and thawing cells in scale. Experience harvesting HEK, CHL and CHO cell lines in large scale using T225, rollerbottles and cell factories is required. The successful candidate must be able to work in a team environment and have weekend work availability.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
San Diego |
CA |
11/19/2009
|
| Research Scientist I (Medicinal Chemistry) |
| Minimum Requirements
? Ph. D. in organic synthesis with 0-3 years of productive, relevant post-doctoral experience or
? MS in organic synthesis with 3+ years of productive pharmaceutical experience or
? BS in organic chemistry with 6+ years of productive pharmaceutical experience
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
San Diego |
CA |
11/19/2009
|
| Research Scientist II (Medicinal Chemistry) |
| Minimum Requirements
? Ph. D. in organic synthesis with 2-5+ years of productive, relevant post-doctoral experience or
? MS in organic synthesis with 5+ years of productive pharmaceutical experience or
? BS in organic chemistry with 8+ years of productive pharmaceutical experience
Vertex Pharmaceuticals |
| BD (Becton, Dickinson and Company) |
San Diego |
CA |
11/20/2009
|
| QA Inspector I |
| See above |
| BD (Becton, Dickinson and Company) |
San Diego |
CA |
11/20/2009
|
| Scientist II - Molecular Biology |
| See above |
| Biogen Idec, Inc. |
San Diego |
CA |
11/20/2009
|
| Associate Scientist II, Molecular Discovery |
1 to 5 years laboratory experience.
A solid understanding of the fundamentals/theory of chromatography.
Excellent written and oral communication skills.
Good computer skills.
Experience with FPLC and/or preparative HPLC a plus. |
| Biogen Idec, Inc. |
San Diego |
CA |
11/20/2009
|
| Scientist II, BioPharm Develop |
| A Ph.D. in Biochemistry/Chemistry/Pharmaceutics/Chemical Engineering or a related discipline with a minimum of two years biopharmaceutical industry experience or relevant postdoctoral experience is required. The candidate should have excellent laboratory, computer, documentation, communication and organizational skills. Experience with protein formulation and analysis is required. |
| 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 |
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. |
| 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 |
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! |
| Astellas Pharma, Inc. |
Saint Louis (1U040202) |
MO |
11/19/2009
|
| Sr. Professional Representative, Urology - Saint Louis, MO |
| REQUIREMENTS:-3+ years pharmaceutical selling experience including 1 years promoting specialty products -Extensive knowledge of sales processes and pharmaceutical products and industry-Excellent communication, facilitation and presentation skills-Can do approach and very high motivational and persuasion skills-Proven, consistent sales record -A BA/BS degree |
| Biogen Idec, Inc. |
Sacramento |
CA |
11/20/2009
|
| Area Business Manager, Neurology - Sacramento CA |
| 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 |
Sacramento |
CA |
11/19/2009
|
| Lab Specialist (Northern California) |
| 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 Northern California. 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. |
RTP |
Durham |
11/19/2009
|
| Bio-Process Technician |
| Education: Bachelor degree in Life Science or Engineering OR Associates degree in Life Science or Engineering and 2 years experience working in the FDA regulated industry. Required:Must be able to lift 50 lbs Must be willing to be vaccinated/blood tested for titer for products manufactured within the facility Must be flexible to work different shifts Preferred:Experience in biological and/or vaccine processing preferred Experience performing aseptic/sterile operations Experience with GMP's (Good Manufacturing Practices) Mechanical aptitude and ability to analyze equipment and take appropriate corrective action 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 # PRO007545 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. |
RTP |
Durham |
11/19/2009
|
| Validation Manager - Formulation and Filling |
| Qualifications:Minimum of a B.S. in Engineering or Science required. M.S. or PhD. in Engineering or Science will be considered. Preferred fields of study include Chemical Engineer, Biochemical Engineer, or Biological Sciences. Minimum of 8 years with all or some of experience in a sterile validation or Quality experience required (can be obtained through a combination of post-graduate education and work-related experience). Minimum of 6 years of the above noted experience is required if MS or PhD degree has been attained Demonstrated leadership and teamwork skills, excellent analytical abilities, proven written and verbal communications skills. Experience preparing regulatory submissions and managing interactions during regulatory inspections required. Ability to gain cross-functional consensus and skilled in conflict resolution. Knowledge of PDA Technical Reports, active member of PDA or other recognized industry group, is preferred. 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 # CHE002102. 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. |
RTP |
Durham |
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 # ADM003878. 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. |
RTP |
Durham |
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 # ADM003888. 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. |
RTP |
Durham |
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 # ADM003918. 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. |
RTP |
Durham |
11/19/2009
|
| Operational Coach- Manufacturing Maintenance Leader |
| Required:Minimum of 6 years experience in a manufacturing maintenance role within a GMP facility. Minimum 4 years coaching/supervisory experience Bachelor degree in Engineering or Science Asset:Vaccine/sterile experience Plant maintenance, project engineering and/or operations experience Computer Maintenance Management System (Maximo) SAP 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 # MAN000272. 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. |
RTP |
Durham |
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 #ADM003942. 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. |
RTP |
Durham |
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 # CHE001998. 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. |
RTP |
Durham |
11/19/2009
|
| Merck Technical Rotation Program |
| This position requires candidate to be currently enrolled in a BS program in Chemical Engineering, Biochemical Engineering, BioMedical Engineering (process option), Chemistry/ Biochemistry, Biology/ Microbiology. 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 # CHE002035. 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. |
RTP |
Durham |
11/19/2009
|
| Engineer |
| This position requires candidate to be currently enrolled in a BS program in Mechanical, Industrial, Electrical Engineering 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 # ENG002103. 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. |
RTP |
Durham |
11/19/2009
|
| Instrumentation Technician |
| Required:High School Diploma or GED Effective calibration/troubleshooting skills Ability to communicate and work in a highly effective team environment Ability to manage multiple priorities and advance several tasks in parallel Demonstrated mechanical aptitude Operation/use of general hand and power tools, instruments and testing apparatus common to the electronic and instrumentation fields Ability to read P&ID's, electrical drawings, blueprints, PLC ladder logic, etc Asset:Experience in aseptic or GMP/regulated manufacturing environment Ability to work with and troubleshoot computer control equipment, including Programmable Logic Controllers (PLCs) and Distributed Control Systems (DCS) 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 # PRO007495. 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. |
RTP |
Durham |
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 # CHE001968. 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. |
RTP |
Durham |
11/19/2009
|
| Operations Coach - Cap & Inspect Production Leader |
| Required: Minimum 2 years coaching/supervisory experience. Minimum 4 years experience in a manufacturing role in an FDA regulated environment Bachelor Degree in Engineering or Science field Asset:Manufacturing experience with automated vial capping and/or inspection equipment 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 # MAN000389. 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. |
RTP |
Durham |
11/19/2009
|
| Chemist |
| This position requires candidate to be currently enrolled in a BS 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. 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 # CHE002018. 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. |
RTP |
Durham |
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 # CHE001988. 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. |
RTP |
Durham |
11/19/2009
|
| Production Technician |
| Required: HS Diploma/GED 3 years experience in a manufacturing environment with a responsibility for mechanical troubleshooting and repair of automated equipment. Ability to work in a highly effective team environment Strong communication (written/verbal) skills Ability to manage multiple priorities and advance several tasks in parallel Ability to work with and troubleshoot computer control equipment including Programmable Logic Controllers (PLC) and/or Distributed Control Systems( DCS) Basic computer fluency (internet browsers, e-mail, word processing)Asset:Associate or Bachelor degree in technical field Bioworks certificate Completed coursework in biotechnical field Experience in clean room or GMP/regulated manufacturing environment 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 #PRO007356. 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. |
| Agilent Technologies, Inc. US |
Roseville |
CA |
11/20/2009
|
| Service Tech Coordinator - Career |
| Position requires:
? Electronics degree, Military Certificate, or equivalent experience required.
? Experience in the electronic instrumentation repair/calibration industry
? Ability to work with minimal supervision and interface effectively with fellow team members, customers and management
? 1+ years direct experience in calibration, diagnosis, troubleshooting and repair to the assembly/component level of Agilent Spectrum Analyzers is highly desired
? Strong abilities in use of technical manuals and schematics
? Competent Computer skills
? Knowledge of Total Quality Methodologies
? Direct experience on Agilent instrumentation and automated calibration systems is preferred
? PMEL/Metrology background is a plus
Geo Location: Roseville, CA
~cb~11/06/09 |
| sanofi pasteur |
Rockford |
IL |
11/19/2009
|
| Vaccine Sales Representative - Rockford, IL |
| 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 |
| Astellas Pharma, Inc. |
Rochester (5PP40401) |
MN |
11/19/2009
|
| Executive Representative, Hospital - Rochester, MN |
| THE SUCCESSFUL CANDIDATE FOR THIS ROLE WILL HAVE:* BA/BS degree or equivalent applicable medical or technical degree * 4 years pharmaceutical or healthcare selling experience, including 2 yrs promoting hospital or immunology products (Hospital, Immun, or Cardio)* Extensive knowledge of sales processes and pharmaceutical products and industry* Excellent communication, facilitation and presentation skills* Can do approach and very high motivational and persuasion skills* Proven, consistent sales record * Travel commensurate with territory size * Residence within assigned territory is requiredIf you are looking for a company where you can truly make a difference and have the opportunity to develop professionally and personally, Astellas may be the place for you. |
| 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 |
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 |
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. |
| 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 |
| BD (Becton, Dickinson and Company) |
Research Triangle Park |
NC |
11/20/2009
|
| Engineer |
| See above |
| BD (Becton, Dickinson and Company) |
Research Triangle Park |
NC |
11/20/2009
|
| Global Business Systems Analyst -Manufacturing Execution System Implementation |
| See above |
| BD (Becton, Dickinson and Company) |
Research Triangle Park |
NC |
11/20/2009
|
| Software Engineer |
| See above |
| sanofi pasteur |
Red Bank |
NJ |
11/19/2009
|
| Vaccine Sales Representative - Red Bank, NJ |
| 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 |
Raynham |
MA |
11/19/2009
|
| Polish Operator I |
| A minimum of a High school diploma, G.E.D. or equivalent required. A minimum of 1 year of experience working in a machine shop or production line environment, machining precise finished products is required. Experience working in a Medical Device manufacturing environment preferred. Experience working in a Good Manufacturing Practice (GMP) or other regulated environment preferred. Experience working in an environment that has gone through Lean process changes preferred. The ability to be flexible to change and support change during a Lean process transformation is required. Grinding or buffing experience preferred. Basic mechanical skills required. Experience with routine machine inspection preferred. Experience with measuring devices preferred. Knowledge of blueprint reading and geometric tolerance dimensions preferred. Basic computer skills required. The ability to work independently and in a team environment is required. Ability to communicate effectively (read, write, and speak) in English is required. Basic math skills, with the ability to add, subtract, multiply, divide, compute percentages and work with decimals required. The ability to perform and record measurements with drop indicators, venires and gauges is required. The ability to stand and/or walk more than 50% of the time is required. Ability to lift up to 25 pounds unaided is required. Must be able to work 3rd Shift (9:30 PM - 6:00 AM, Sunday through Thursday). The ability to work occasional overtime and holidays 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 |
Raynham |
MA |
11/19/2009
|
| Platform Director |
| A minimum of a BS/BA degree is required with an MBA or other advanced degree highly preferred. A minimum of 6 years of total business experience is required, with at least 2 of those years in the following areas: a combination of R&D and marketing experience, brand or strategy marketing, or new product development project management is required. Medical Device experience is highly preferred. Experience in developing and presenting business strategies is required. Must have the ability to influence without authority across multiple levels. This position requires someone to be both strategic and tactical. Experience with financial modeling is preferred. Must possess demonstrated analytical skills. Must have experience with Voice of the Customer (VOC) and/or Job Outcomes Constraints (JOC) techniques and the ability to translate them. Must be able to utilize both written and oral communication skills to produce effective marketing materials. Must have experience making effective presentations to small and large groups at all levels. Must have experience working in cross functional teams, and be able to engage and get buy in from key internal stakeholders and drive teams towards consensus on product needs/opportunities. This position requires approximately 30% travel primarily domestic with some 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! |
| Johnson & Johnson Family of Companies |
Raynham |
MA |
11/19/2009
|
| Supplier Quality Engineer I |
| A minimum of a Bachelor's degree is required, preferably in an Engineering, Life Science, or a related discipline. This position will require a minimum of 0-2+ years experience (including internships, co-ops, or other related experience). A Masters/Advanced degree is an asset. Other experience that is an asset, but not required, will include: Experience in a highly regulated industry is an asset. Experience in the Medical Device industry is preferred. Experience in the Pharmaceutical industry is an asset. FDA and ISO regulations knowledge is an asset. Auditing knowledge is an asset. Strong communication, teamwork, and problem solving skills will be needed. Knowledge in root cause analysis skills are an asset. Experience or knowledge with machining manufacturing processes and injection molding an asset. Six Sigma, Lean, or ASQ Certification and trainings an asset. This position will require up to 20% travel. |
| Johnson & Johnson Family of Companies |
Raynham |
MA |
11/19/2009
|
| Polish Operator Lead |
| A minimum of a High school diploma, G.E.D. or equivalent required. Vocational designation or training in preferred. A minimum of 3 years of experience working in a machine shop or production line environment, machining precise finished products required. A minimum of 1 year of grinding and/or buffing experience preferred. Experience working in a Medical Device manufacturing environment preferred. Experience working in a Good Manufacturing Practice (GMP) or other regulated environment preferred. Prior experience in a leadership role (i.e. team lead, group lead) preferred. Training experience preferred. Experience working in an environment that has gone through Lean process changes preferred. The ability to drive change as a change agent in a Lean environment required. Basic mechanical skills required. Prior inspection experience required. Knowledge of blueprint reading and geometric tolerance dimensions preferred. Basic computer skills required. Experience collaborating in a team environment required. Ability to communicate effectively (read, write, and speak) in English is required. Must have strong interpersonal skills to work with people of the production floor. Basic math skills, with the ability to add, subtract, multiply, divide, compute percentages and work with decimals required. The ability to perform and record measurements with drop indicators, venires and gauges is required. The ability to stand and/or walk more than 50% of the time is required. Ability to lift up to 25 pounds unaided is required. Must be able to work 3rd Shift (9:30 PM - 6:00 AM, Sunday through Thursday). The ability to work occasional overtime and holidays 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 |
Raynham |
MA |
11/19/2009
|
| Staff Engineer/ Black Belt Process Driver |
| BS- Engineering, is required for this role and a Master's Degree in Engineering would be a plus. A strong technical background is also required.Black Belt certification in Design Excellence mandatory. A Master Black Belt is an asset in this role.2 years as certified Black Belt leading and delivering significant new product development projectsMedical device experience a significant plus. Experience in a regulated industry is required.Ability to align board members, cross-functional directors/managers and engineers to drive organizational change through effective leadership, interpersonal and communication skillsKnowledge of New Product Development, taking a product from concept through commercialization is a requirement.Ability to teach design excellence tools is required and the ability to help others complete Black and Green belt training is an asset.Ability to prioritize and complete multiple projects on time and within assigned resource constraints. 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 |
Raynham |
MA |
11/19/2009
|
| Disposable Products Group Lead (2nd Shift) |
| Minimum of a High school Degree or equivalent required. Minimum 5 years of business experience preferably in Production, Operations, Procurement, Manufacturing, Supply Chain and/or related discipline. Previous experience working in a regulated environment required. This is a second shift position and requires the ability to work second shift (3:30 PM to midnight). This position requires the ability to work overtime (third shift) and weekends as needed. This position is located in Raynham, MA and does not provide relocation assistance or transportation assistance. Ability to read and write English required. Demonstrated leadership qualities required. Ability to effectively communicate and work with all Operators and Production Support Associates required. Proven track record of success is required. Ability to continuously monitor and meet daily quality standards, production metrics and efficiencies while complying with QSR, ISO and Safety regulations is required. Ability to interpret & follow detailed process specifications with no supervision is required. Ability to work in an open work area and in a clean room environment on a daily basis is required. Ability to work well independently and on small or large teams is required. Intermediate to expert level proficiency in Microsoft Office (Outlook, Excel and Word) required. Ability to lift 25 pounds and to stand and sit for extended periods of time is required. Ability to prioritize and coordinate multiple tasks and projects in an environment of competing priorities is required. Previous experience working with MRP or ERP system preferred. Experience managing workflow processes and daily production schedules strongly preferred. Experience working in Medical Device, Disposables and/or Clean Room environment is highly 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 Family of Companies |
Raynham |
MA |
11/19/2009
|
| Program Manager |
| BS/BA required. A minimum of 2 years experience working in organizational learning, seminar planning or medical education required. Healthcare experience preferred. Must work well in a team environment. Ability to make decisions independently and seek guidance where appropriate required. Proven written and oral communication skills required. Strong time management skills required. Approximately 30% travel required. |
| Johnson & Johnson Family of Companies |
Raynham |
MA |
11/19/2009
|
| Director, Market Access |
| A minimum of a Masters degree in biomedical science, health service research, or economics is required. A minimum of 8 or more years experience in the Medical Device, Pharmaceutical or Health plan industry is required with track record of scientific and business impact success. Ability to develop and communicate economic models and analyses required. Knowledge of reimbursement across treatment settings (i.e., hospital inpatient, hospital outpatient, physician's office, long term care, home health, etc.) is required. Previous reimbursement/market access experience working with US and global payors is required. Understanding process and decision-making criteria for evaluating new technologies and for setting reimbursement rates is a must. Experience in leading cross- functional teams to deliver and communicate evidence generation strategy and customer requirements. Demonstrated ability to provide constructive and innovative input into complex problems. 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. 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. A minimum of 30% 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 |
Raynham |
MA |
11/19/2009
|
| Document Management Supervisor |
| Minimum of a Bachelor Degree with 4 years of experience in Quality Systems and Electronic ERP, Document and Change Management Systems in a regulated industry OR an Associate Degree with 8 years of experience in Quality Systems and Electronic ERP, Document and Change Management Systems in a regulated industry required. Supervisory experience required. Experience working with MS Office (Outlook, Word and Excel) required. Ability and willingness to assess and learn to use new tools and technologies to accomplish work are required. Ability to identify and apply quality and compliance regulations, standards, and requirements as they apply to Document Management is required. Excellent organizational skills required. Must be conscientious and attentive to detail, balanced with big-picture thinking. Must be resilient, adaptable and deal effectively with change. Strong verbal/written communications skills are required. Strong time management skills, including the ability to multi-task and prioritize work in a dynamic environment are required. Must work efficiently under pressure in order to meet demanding deadlines. Must be able to demonstrate a capacity to influence by expressing and promoting ideas, taking a clear stand on issues and making oneself understood and respected. Must be comfortable with ambiguity and uncertainty. Strong team-building skills, with the ability to function as a team player or leader on cross-functional teams is required. Ability to set tactical direction to support strategic initiatives required. Experience working in medical device industry is preferred. Experience managing transformational change and authoring and maintaining procedures and work instructions is preferred. Experience working with SAP ERP systems 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 Family of Companies |
Raynham |
MA |
11/19/2009
|
| Mechanic II, Production Maintenance |
| A minimum of a High School diploma, G.E.D. or equivalent required. Technical school preferred. A minimum of 4 years of related equipment maintenance experience and/or training is required. Experience maintaining CNC Mills, Lathes, Grinders, EDMs (Electrical Discharge Machines) and ABB Robotics required. Experience maintaining Fanuc and Siemens CNC controllers preferred. Experience maintaining mechanical, electrical/electronic, hydraulic and pneumatic equipment components required. Basic computer skills required. Must be a certified Forklift and Power Pallet Jack Operator or be willing to become certified. Must be able to supply own hand tools (i.e. screw drivers, socket wrenches, etc.). Must be able to communicate (read, write and speak) effectively in English. Must have strong communication and interpersonal skills. The ability to left heavy loads, stand and/or walk more than 90% of the time and perform twisting and turning activities required. The ability to work in confined or awkward areas, climb ladders and work from heights required. Must have a valid driver's license. Must be a team player and be able to work with minimal technical supervision. Must be able to work 2nd shift (3:30 pm - 12:00 am). This ability to work overtime, including weekends, and to participate in on-call rotation is required. This position requires the incumbent to submit to and pass periodic and random drug testing as a condition of initial and continued employment. 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 |
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 |
Raritan |
NJ |
11/19/2009
|
| I/T SOX PROGRAM MANAGER |
| Experience in design and implementation of COBIT framework for SOX and Assessment within large, complex IT environments. Preferred experience with implementation in Fortune 500 Company.Bachelor's degree required. Advanced degree preferred. 10+years business experience required; 5+ years IT Compliance, information security, and/or audit experience in Big4 environment required.Subject matter expertise in SOX Compliance and Controls with experience interfacing with various auditing/regulatory entities required.External SOX IT Audit experience required.Experience performing "top-down" IT Risk Assessments for systems impacting internal controls over financial reporting. Experience in Risk ManagementExperience training and educating audit staff and control owners on SOX compliance requirements.Experience writing policies and managing compliance documents.Knowledge of IT systems and process analysis tools.Awareness of common security technologies.Demonstrated management skills building and motivating teams in an environment undergoing high amounts of change. |
| Biogen Idec, Inc. |
Raleigh/Durham |
NC |
11/20/2009
|
| Scientist I, Stability |
Minimum of 3 years direct experience in stability / formulation of biological and/or small molecule products in the Pharmaceutical industry, with 6+ years industry experience.
PhD with 6+ years industry experience preferred, or BS/MS degree in Biology, Chemistry, Biochemistry, Chemical/Biochemical Engineering, or related disciplines with equivalent experience. |
| Johnson & Johnson Family of Companies |
Raleigh |
NC |
11/19/2009
|
| Senior Quality Assurance Engineer |
| A minimum of a Bachelor's degree in Engineering, Science, Technology or a related discipline is required, with a minimum of 5+ years experience in a highly regulated industry required, with experience in the medical device or pharmaceutical industry preferred. A minimum of 3+ years experience as a Quality Engineer is required. CQE or equivalent certification is an asset. Experience with Chemical Processing, Chemistry, or in a related lab area is an asset. Thorough understanding of FDA Quality System Regulation, MDD, ISO 13485:2003, quality engineering methodology, and quality management principles are an asset. Working knowledge of Standards applicable to Medical Device Industry are an asset. Experience with medical device product design and manufacturing processes is an asset. Knowledge of statistical tools and techniques is an asset. Experience in analytical problem solving is an asset. Proven accomplishment in Quality System Auditing is an asset. FDA Notified Body experience as a team member is an asset. Personal computer and software applications experience, including e-mail, Internet applications, Word processing, spreadsheet, and database work is required. Statistical Analysis program, Minitab, or other statistics software experience is required. Must be able to work within a team and handle multiple tasks. Experience with dimensional tools (e.g. rulers, optical comparators, calipers, micrometers, pin gauges) and balances/scales is an asset. This position is located in Raleigh, NC. 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. |
| 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. |
| 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. |
| Merck & Co., Inc. |
Rahway |
NJ |
11/19/2009
|
| Lab Animal Vet |
| Education Requirement: DVM or VMD Required:At least 2 years post-doctoral training or experience in laboratory animal science is required along with team orientation. Must possess strong leadership and interpersonal skills. Must communicate effectively with all personnel within department and members of the Merck Research Lab Research community. Demonstrates ability to coordinate activities and careers of subordinates. Desired:Diplomate status, ACLAM is preferred or relevant specialty with an AVMA recognized veterinary specialty organization. At least 4 but no more than 8 years experience or MS/PhD in the specialty of laboratory animal care. 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 # LAB000108. 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 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. |
Rahway |
NJ |
11/19/2009
|
| Project Scientist |
| Education:BS in Biological Sciences Required. MS in Biological Sciences Preferred Required experience: 3 years post-bachelors degree experience in supply for therapeutic proteins/vaccines/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 #PRO007555. 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. |
Rahway |
NJ |
11/19/2009
|
| Associate Director Clinical Research |
| Required:-An M.D or M.D./Ph.D, plus Board Certification or Eligibility is preferred. Must have experience in industry or academia Desired:-Previous clinical development experience preferably in biologics or in therapeutic areas of arthritis, clinical immunology, anemia or hematology. 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 # CLI002031. 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. |
Rahway |
NJ |
11/19/2009
|
| Assoc Dir / Dir Clin Research, Rotation |
| Education:M.D or M.D./Ph.D; Ph.D with substantial post-doctoral experience will also be considered Required:Demonstrated record of scientific scholarship and achievement A proven track record in clinical medicine and background in biomedical research is essentialStrong interpersonal skills, as well as the ability to function in a team environment are essentialPreferred:Prior specific experience in clinical research and prior publication is hightly desirableBoard Certification or Eligibility is preferredConsistently 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 # CLI001986. 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. |
Rahway |
NJ |
11/19/2009
|
| Research Associate |
| Education requirements:Must currently possess a PhD or expect to earn a PhD within the next 9 months OR must have a Bachelor's or Master's Degree with at least 5 years of research experience and 2 first-author publications. A concentration in one of the following studies is required; mathematics, computational biology, computer science, statistics, or another area applying math, statistics, and/or computer science to biology, biotechnology, chemistry, genetics, biochemistry, or pharmacology. Required: The position requires advanced and thorough scientific knowledge related to the above-mentioned areas of expertise. Must have the ability to plan, recommend and complete research programs of major divisional importance. The incumbent must be capable of motivating and training junior scientists and offering counsel to peers within the Division. Experience in several and extensive knowledge in one or more of the following areas is required: discrete and numerical algorithms, machine learning and automated pattern recognition, signal and/or image processing, computational biology, mathematical analysis and modeling, differential equations, mathematical programming, probability, stochastic processes, scientific software engineering, optimization, parallel algorithms, complexity theory, or knowledge representation. Mature communication and interpersonal skills are required. Preferred: Post-graduate research experience or some combination of directly relevant R&D work and training could also be an asset, especially if relevant to solving problems in the pharmaceutical/biotechnology/biomedical industry. 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 # INF003860. 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 |
| Radiometer America, Inc. |
Quebec |
C09 |
11/19/2009
|
| Sales Representative |
| •Bachelor’s degree in respiratory, biology, or chemistry preferred.
•2 to 5 years in medical capital equipment sales experience with proven accomplishments clinical lab or similar work. Immunoassay experience required.
•Qualified candidate will have good organization, time management and presentation skills.
•Ability to communicate at all levels internally and externally with customers.
•Extensive travel – 50%+
|
| 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! |
| Johnson & Johnson Family of Companies |
Princeton |
NJ |
11/19/2009
|
| POSTDOCTORAL SCIENTIST |
| A Ph.D. in biological sciences is required. Strong working knowledge of molecular and cellular mechanisms, signal transduction, receptor biology, and cell-cell communication is required. Hands-on experience with molecular and cellular biology techniques, mammalian tissue culture and microscopy is required. Knowledge of skin biology is desired. Ability to work independently and within a team environment, as well as computer literacy and good communication skills are required. This is a 1 year assignment with potential to extend 1 additional year based on business need. |
| Johnson & Johnson Family of Companies |
Portland |
ME |
11/19/2009
|
| Portland, ME- 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 |
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! |
| 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 |
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 |
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! |
| Johnson & Johnson Family of Companies |
Piscataway |
NJ |
11/19/2009
|
| SAP Global Process Subject Matter Expert - Master Data Management |
| A minimum of a Bachelor's degree is required. A Master's degree is preferred. A minimum of 5 years of experience in manufacturing roles within Operations or Supply Chain is required. A minimum of 2 years of experience within a Master Data Management role is highly desirable. A working knowledge of SAP is required. Experience working in an FDA regulated environment with an emphasis on Validation & Compliance of systems and processes is preferred. Experience working remotely with business partners in a global environment is preferred. Process re-engineering experience is preferred. Experience working with multiple franchises and sectors in a highly matrixed environment is preferred. Experience with any of the following is preferred: Process Flow Diagrams, Business user requirements and Documentation. Professional Certification with CPIM, CSCP, Six Sigma Black or Green Belt is preferred. This position will require up to 20% of domestic travel. This position will be based 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! |
| Johnson & Johnson Family of Companies |
Piscataway |
NJ |
11/19/2009
|
| Sr. Analyst, E-Commerce |
| A minimum of a Bachelors degree is required. A minimum of 5 years business experience is required, preferably from a Supply Chain, Operations or Production environment. A minimum of 3 years EDI and/ or Information Technology experience is required. Experience with SAP is highly desired. Experience working with ANSI X-12/ EDIFACT EDI standards desired. Knowledge of communication protocols, translation software, applications software, EDI transaction sets and Value Added Networks would be preferred. Prior experience with XML would be an asset. Ability to translate business requirements into technical specifications is required. Project management experience is highly desirable. Experience working with multiple franchises and sectors in a highly matrixed environment is preferred. Must have a proven record of excellence in multi-tasking, follow-up and execution of assignments against commitments. Outstanding time management, project management and prioritization skills are required. He/she must have strong analytical skills with the ability to identify and analyze problems, issues, situations and recommend/apply appropriate solutions. Must be proficient in utilizing the MS Office Suite applications (Word, Excel, PowerPoint, Outlook etc). This position will require up to 5% travel, domestically, as needed by business. This position will be based 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! |
| Johnson & Johnson Family of Companies |
Phoenix |
AZ |
11/19/2009
|
| Phoenix, AZ: 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! |
| Johnson & Johnson Family of Companies |
Phoenix |
AZ |
11/19/2009
|
| CLINICAL EDUC SPEC ULTRASOUND Phoenix, AZ |
| A minimum of 3 years clinical experience in echocardiography is required. Registered Diagnostic Cardiac Sonographer (RDCS) or Registered Cardiac Sonographer (RCS) certification or eligibility to sit for certification is required.. Excellent presentation and training skills; outstanding interpersonal and relationship-building Bachelor's Degree (or equivalent), RN, PA-C, CNP is required. Solid organizational and time management abilities required as this is a field-based position. Ability to travel up to 75% of the time in the region is required. Ability to wear protective lead in the lab is required. A valid US driver license and clean driving record 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 |
Phoenix |
AZ |
11/19/2009
|
| Southwest Region: 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 |
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! |
| 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! |
| 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! |
| 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
|
| CommonHealth |
Parsippany |
NJ |
11/20/2009
|
| Medical Director |
| Requirements:
2+ years experience in patient care or medical education
Advanced degree in biomedical sciences (PharmD, PhD, MD)
Developing educational concepts and content through critical analysis of data, distilling complex technical information for a variety of medical audiences, working with opinion leaders
Knowledge of CME procedures
Writing proposals
Editing documents
Clinical research and publication experience is a plus.
Ability to provide independent medical direction
Strong written and verbal communication and presentation skills.
Software: Microsoft Word, PowerPoint, reference database programs such as Refman
Familiarity or interest in pharmaceutical marketing
Must work well in a team-oriented environment
Ability to meet deadlines while working on multiple, parallel projects
Develop solid understanding of the market and goals advocated by the medical and marketing clients
We are an equal opportunity employer.
|
| CommonHealth |
Parsippany |
NJ |
11/20/2009
|
| Medical Writer |
| Knowledge and Skills
Doctoral level education in biomedical sciences preferrably (PhD, PharmD, MD) oncology experience required
Knowledge of assigned therapeutic areas
Experience writing peer-reviewed articles, distilling complex technical information for a variety of medical audiences
Familiarity with RefMan or similar database program, Word, PowerPoint
Familiarity with AMA style writing
Ability to write high-quality scientific articles
Demonstrated written and verbal communications skills
Ability to work as a team member
Problem Solving
Balancing work quality with timelines
Adopting the writing style to the target audience
Managerial Direction
Make decisions regarding content and style in consultation with program management and account management
Self management to adhere to agreed T&E schedules, budgets, and to alert team to potential deviations and overages
We are an equal opportunity employer
|
| CommonHealth |
Parsippany |
NJ |
11/20/2009
|
| Medical Oncology Copywriter |
| Knowledge and Skills
Doctoral level education in biomedical sciences preferrably (PhD or PharmD) oncology experience required
Knowledge of assigned therapeutic areas
Familiarity with AMA style writing
Ability to write high-quality scientific articles
Demonstrated written and verbal communications skills
Ability to work as a team member
Problem Solving
Balancing work quality with timelines
Adopting the writing style to the target audience
Managerial Direction
Make decisions regarding content and style in consultation with program management and account management
Self management to adhere to agreed T&E schedules, budgets, and to alert team to potential deviations and overages
We offer a competitive salary, excellent benefits, and a great working environment.
We are an equal opportunity employer.
|
| sanofi pasteur |
Palo Alto |
CA |
11/19/2009
|
| Vaccine Sales Representative - Palo Alto, CA |
| 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 |
Omaha |
NE |
11/19/2009
|
| Omaha, Nebraska - 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! |
| Radiometer America, Inc. |
Northern California |
CA |
11/19/2009
|
| Sales Representative |
| •Bachelor’s degree in respiratory, biology, or chemistry preferred.
•2 to 5 years in medical capital equipment sales experience with proven accomplishments clinical lab or similar work. Immunoassay experience required.
•Qualified candidate will have good organization, time management and presentation skills.
•Ability to communicate at all levels internally and externally with customers.
•Extensive travel – 50%+
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.
|
| Teva Pharmaceuticals USA |
North Wales |
PA |
11/20/2009
|
| Business/Market Research Analyst |
|
| 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 |
North Wales |
PA |
11/20/2009
|
| Sr. Manager, Network Administration & IT Security |
|
| Teva Pharmaceuticals USA |
North Wales |
PA |
11/20/2009
|
| Talent Development Specialist |
|
| Agilent Technologies, Inc. US |
Newport |
DE |
11/20/2009
|
| Chemical Process Engineer |
| Qualifications
Minimum of 4 years experience in chemical process manufacturing
Bachelors or Masters Degree in chemical engineering or chemistry
Demonstrated ability to apply chemical process fundamentals
Extensive cross-functional team experience with demonstrated excellent teamwork skills
Demonstrated success with process transfer and scale-up from R&D
Previous manufacturing experience in an ISO9000 environment
Demonstrated success improving process performance with respect to quality, rate, and yield
Proven ability to find successful solutions to multiple problems of varying scope and complexity
Demonstrated ability to work across multiple functions leading and managing projects
Excellent written and oral communication skills
Desired Qualifications:
5 to 8 years of experience
Experience with batch chemical processing
Experiences applying LEAN principles in a manufacturing environment
Experience with colloidal science - experience with colloidal silica a plus
Experience working within a Six Sigma organization with Green Belt or Black Belt certification
~cb~10/28/09 |
| Strategic Diagnostics Inc. |
Newark |
DE |
11/19/2009
|
| Senior Scientist-Transfection Specialist |
| Demonstarted broad technical expertise in the area of mammalian cell transfections, both for soluble as well as cell bound protiens.
High level of technical expertise in tissue culture
Ability to design and execute plans, interpret results and summarize findings in the area transfection for optimal protein expression for immunization and screening
Prepare and be accountable for timelines
Ability to work well independently as well as part of mutidisciplinary teams
Strong communication skills
MS or PhD preferred with 8-12 years experience (excluding school)
A significant portion of the work for this position is at the bench.
|
| Strategic Diagnostics Inc. |
Newark |
DE |
11/20/2009
|
| Field Application Scientist |
| Credentials Required:
· Ph.D level scientist in Molecular Biology, Immunology or related sciences
· At least 5 years of experience generating of monoclonal and polyclonal antibodies, and/or production of antibodies in vitro and in vivo (ascites) and maintaining cell lines.
· Scientist/consultant with industrial expertise in research & development related to hybridoma technology and/or immunoassay development.
· Proficient or general understanding of Antibody Methodology (mono/polyclonal) such as:
-Rabbit, mouse, hamster or rat handling techniques;
-Mouse ascites fluid and/or hollow fiber bioreactor production of monoclonal antibodies;
-Lymphocyte cell fusions,
-Tissue culture and media formulations,
-Cell freezing techniques,
-Hybridoma fermentation and antibody purification;
-ELISA, RIA, IFA, Western Blot Analysis. MesoScale Platform, IHC techniques; Flow Cytometry (FACS)
-Cell transfections and Protein expression experiments
· Experience and high degree of comfort doing technical presentations
· Energetic, resourceful and highly motivated. Ability to think strategically and work independently.
· Ideally has commercial acumen and understand sales process. |
| Strategic Diagnostics Inc. |
Newark |
DE |
11/19/2009
|
| Scientist III |
| Qualifications: (Knowledge, Skills and Abilities: Education, Experience, Job Skills, Equipment Skills, and Certifications)
1. B.S/B.A. in Biology, molecular biology, Chemistry, biochemistry/ microbiology/ immunology/ medical technology field with 5+years. MS or PhD generally required for this level with 1-2 years of experience.
2. Strong knowledge of QSR, cGMP and ISO regulations and guideline
3. Fully knowledgeable of Instrumentation used in molecular biology.
4. Demonstrated skill in the areas of protein purification and analysis; such as IMAC, Gel filtration, western blot.
5. Demonstrated skill in the areas of DNA manipulation; such as PCR and gene construction, sub-cloning and sequence analysis.
Supervisory Responsibilities:
May manage a team of scientists and technicians performing, training, coaching and aid in quarterly and yearly performance reviews, conducts disciplinary discussions as appropriate.
Abilities:
1. Thorough understanding of molecular biology and protein biochemistry.
2. Must be familiar with accepted industry practices and regulations
3. Maintain broad knowledge of current scientific theories and practices.
4. Able to multitask
5. Able to work independently and lead a team of scientists
6. Able to organize and prioritize tasks for his/her self and others
7. Able to resolve problems with others
8. Good verbal and written communication
9. Develops SOP’s
10. Documents coaching
Work Environment / Other Requirements:
Works in a variety of lab environments that could lead to exposure to heat, cold, dry air, chemicals, odors and humidity. Ability to lift 50 pounds required
|
| Strategic Diagnostics Inc. |
Newark |
DE |
11/20/2009
|
| Senior Scientist-Process Engineer |
| Experience in lateral flow, immunoassay, bioluminescence and other bioassays is preferred. MS or PhD generally required for this level with 8-12 years of experience. Individual must demonstrated technical expertise in a related business or field. Must be familiar with accepted industry practices and regulations. Prefer experience in a Food Industry, or Biopharmaceutical/Pharmaceutical Manufacturing environment. |
| Strategic Diagnostics Inc. |
Newark |
DE |
11/20/2009
|
| Manufacturing Manager |
|
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Manufacturing Manager
Location: Newark-Pencader
Job Code: 51
# of openings: 1
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Description
The Manufacturing Manager is responsible for planning, organizing, staffing directing and controlling production. The manager sets priorities, coordinates the scientists and operators work schedules to meet production requirements while maintaining a high quality standard. Leads continuous improvement programs to increase yield and reduce variation. Helps lead technical troubleshooting and root cause analysis efforts to reduce cost and improve output quality. The manager is an integral part of internal product/process redesigns, new product transfers from R&D and the integration and process transfer of external product/process acquisitions.
Responsibilities and Duties:
1. Manages and coordinates the Scientist/Operator production activities and schedules. Meets job schedules with acceptable quality.
2. Hires new employees and is responsible for operator training & certification, establishes standards of performance, conducts employee performance appraisals and on going coaching. Conducts corrective actions when disciplinary action is required and enforces company policies, rules and regulations.
3. Must be able to achieve completion of objectives through mentoring and coaching others..onitors and measures the department performance, strives for continual improvements in productivity and ways to increase capacity and reduce cost.
4. Monitors and measures the department performance, strives for continual improvements in efficiencies and reductions in variation and costs.
5. Takes ownership for the quality of products produced and services performed.
6. Is dedicated to reducing process variation and champions the use of statistical process control (SPC) and formal problem solving tools across all operations, trains employees in quality theory and practice, writes and modifies procedures to confirm to quality standards and maintains proficiency in problem solving techniques.
7. Responsible for the managing and replenishment of key custome reagents.
8. Responsible for the accuracy of the MRP system data, Bill of Material and Routings, Syspro standards and the material and labor variances.
9. Determines manufacturing capital and tooling needs. Is knowledgeable of the process specifications in his/her area of responsibility and is dedicated to the reduce process variation.
10. Continually works towards control of key equipment variables and process parameters associated with the lyophilizers, fermenters, centrifuges, balances, coating machines, reel-to-reel sprayer and dippers. Ensures equipment maintenance is appropriate and monitored.
11. Writes and follows standard operating procedures and makes certain paperwork is properly filled out and data collection systems reflect accurate product movements.
12. Is knowledgeable of the process specifications in the area of responsibility.
13. Makes sure process changes are documented before a new process or change is implemented on the production floor.
14. Communicates effectively with the Supply Chain Manager and Sales & Marketing to resolve customer performance problems, participates in customer audits and visits.
15. Complies with and aids in the development of department safety rules, monitors area for hazards, uses proper personal protective equipment (PPE) when required and maintains a safe, clean and organized work area.16. Monitors and maintains supplies, spare/contingency parts and WIP minimums to reduce downtime.
16. Performs other duties as assigned.
Qualifications :
BS/BA in biochemisty/microbiology/engineering field
At least 5 years of management experience in a manufacturing enviornment
Familiar with antibody and or immunoassays processes
Good mechanical and mathematical abilities and the ability to make critical judgments within the production processes.
Familiarity with antibody and/or immunoassay processes.
Computer proficiency- Word, Excel, PowerPoint, and Project expertise is preferred.
Knowledgeable of SPC and the use of data driven problem solving tools.
Good verbal and written communication skills.
Abilities:
Consistently meets production schedule deadlines
Consistently sets and meets production goals
Identifies and resolves production issues.
Establishes and makes changes to process for continuous improvement
Trains staff on process
Excellent organizational skills
Must be able to mutli-task
Must be able to apply priority management skills and assess the risk/benefits of decisions and actions.
Supervisory Responsibilities:
Manages a staff of technical and labor personnel. Responsibilities include interviewing, hiring and training new employees, planning, assigning and directing work, conducts employee appraisals, on-going coaching sessions provides a motivating work environment, enforces company policies, rules and regulations and maintains cooperation with other areas.
Work Environment/ Other requirements:
At SDI our work environment varies significantly from job to job. Ability to lift or move 20 pounds and work/travel throughout plant environment of varied temperatures and humidity; grasp and hold small objects, a full range of motion, and to wear personal protective devices. This position may expose the employee to fumes or airborne particles, biohazards, and toxic or caustic chemicals. Daily contact with employees in other department | |
