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Search Jobs by Category
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Zebrafish Research Associate (BS/MS) |
| Minimum:
? B.S/B.A or M.S. degree in a biological science with a minimum 5 years laboratory research experience
? Proficiency in the use of current molecular biology techniques and cloning strategies, quantitative PCR, site-directed mutagenesis, construction of reporter systems, assessment of protein levels using antibody reagents, and the design and use of various expression vectors
? Experience using gene knockdown, over-expression or microinjection technologies, including RNA interference, to assay the function of pathway activity in.
? Excellent organizational, communication and computer skills.
Preferred:
? General knowledge of zebrafish husbandry
? 1+ years experience in a zebrafish laboratory
? Experience working with a model organism: embryology, genetics and developmental biology principles, whole mount gene expression analysis, phenotypic analysis.
? Familiar with microscopy and imaging. |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| WW Senior Strategic Marketing Manager |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| WW Controller Cell Analysis |
| See above |
| 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! |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Wnt Scientific Associate, Developmental & Molecular Pathways |
| B.S. or M.S. in Biochemistry, Cell Biology or Molecular Biology
Minimum 5 years experience in biochemistry, mammalian cell biology working with various cell lines and/or cell signaling mechanisms
Previous experience with stable cell line production, design and analysis of cell-based assays, transfection and viral transduction technologies and genetic knockdown techniques including RNAi is required.
Proficiency in the use of molecular biology and protein biochemistry technologies, e.g. DNA cloning, Real-time PCR, protein-protein interaction, and enzymatic assays is preferred.
Demonstrated ability to evaluate and implement new techniques and technologies.
Experience mentoring and leading scientific associates.
Must be highly motivated, team-oriented, and have excellent interpersonal and communication skills. |
| Johnson & Johnson Family of Companies |
White Plains |
NY |
11/19/2009
|
| Westchester, NY- Full Line Sales Rep - Ethicon-Endo Surgery |
| To be considered for this role, candidates must meet the following criteria: A minimum of a Bachelors Degree paired with three or more years of sales experience selling to a highly educated/high profile customer base, or internal EES experience with a proven track record of achieving sales & competency objectives as a Sales Representative. The ability to sell in an operating room, lab & hospital environment is required. A valid driver's license issued in one of the 50 States with a clean driving record is required. The ability to travel as necessary, which may include overnight and/or weekends, is required. Medical device sales experience is preferred paired with documented sales results. Individuals must live within the current geography or be willing to relocate to it. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Johnson & Johnson Family of Companies |
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 |
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! |
| Biogen Idec, Inc. |
Cambridge |
MA |
11/20/2009
|
| VP, Regulatory Affairs Syntonix |
Deep functional knowledge and significant experience leading broad range of Regulatory activities with global scope:
â?¢Interfacing with relevant regulatory authorities through all stages of drug development. International Regulatory experience strongly preferred.
â?¢Preparation of major regulatory submissions and supportive amendments or supplements from IND through BLA. Experience with post-marketing commitments and commercial labeling and promotion preferred.
â?¢Direct experience with Orphan Drug, Fast-Track, Priority Review and Accelerated Approval.
â?¢Broad knowledge of international GCP and GMP requirements and the ability to translate market-to-market differences into integrated development approach.
â?¢Assessment of CMC changes, developing comparability protocols based on critical product quality attributes, and translation to clinical planning.
â?¢Good knowledge of evolving RoW Guidelines and Regulations and how to incorporate into global development plans. |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| VP Manufacturing Injection |
| See above |
| BD (Becton, Dickinson and Company) |
Sandy |
UT |
11/20/2009
|
| VP Manufacturing Infusion |
| See above |
| BD (Becton, Dickinson and Company) |
Wilson |
NC |
11/20/2009
|
| Validation Technician II |
| See above |
| 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. |
| BD (Becton, Dickinson and Company) |
Burlington |
NC |
11/20/2009
|
| Validation Engineer I |
| See above |
| BD (Becton, Dickinson and Company) |
Wilson |
NC |
11/20/2009
|
| Validation Engineer |
| See above |
| 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 |
| 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 |
| 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 |
| 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 |
| sanofi pasteur |
Jefferson City |
MO |
11/19/2009
|
| Vaccine Sales Representative - Jefferson City, MO |
| 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 |
| sanofi pasteur |
Gilbert |
AZ |
11/19/2009
|
| Vaccine Sales Representative - Gilbert, AZ |
| 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 |
| sanofi pasteur |
Chicago North |
IL |
11/19/2009
|
| Vaccine Sales Representative - Chicago N, 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 |
| sanofi pasteur |
Charlottesville |
VA |
11/19/2009
|
| Vaccine Sales Representative - Charlottesville, VA |
| BA./B.S. in Immunology, Biology, Business or related field required.
2 years business to business sales or equivalent experience.
Strong oral, written and analytical skills with the demonstrated ability to work in teams.
Strong time management skills
Certifications
Driver's license is required along with a record of safe driving |
| sanofi pasteur |
Chandler |
AZ |
11/19/2009
|
| Vaccine Sales Representative - Chandler, AZ |
| 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 |
| sanofi pasteur |
Champaign |
IL |
11/19/2009
|
| Vaccine Sales Representative - Champaign, 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 |
| sanofi pasteur |
Buffalo |
NY |
11/19/2009
|
| Vaccine Sales Representative - Buffalo, NY |
| BA./B.S. in Immunology, Biology, Business or related field required.
2 years business to business sales or equivalent experience.
Strong oral, written and analytical skills with the demonstrated ability to work in teams.
Strong time management skills
Certifications
Driver's license is required along with a record of safe driving |
| sanofi pasteur |
Blacksburg |
VA |
11/19/2009
|
| Vaccine Sales Representative - Blacksburg, VA |
| BA./B.S. in Immunology, Biology, Business or related field required.
2 years business to business sales or equivalent experience.
Strong oral, written and analytical skills with the demonstrated ability to work in teams.
Strong time management skills
Certifications
Driver's license is required along with a record of safe driving |
| sanofi pasteur |
Astoria |
NY |
11/19/2009
|
| Vaccine Sales Representative - Astoria, NY |
| BA./B.S. in Immunology, Biology, Business or related field required.
2 years business to business sales or equivalent experience.
Strong oral, written and analytical skills with the demonstrated ability to work in teams.
Strong time management skills
Certifications
Driver's license is required along with a record of safe driving |
| sanofi pasteur |
Albany |
GA |
11/19/2009
|
| Vaccine Sales Representative - Albany, GA |
| 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 |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| US Clinical Operations Training Manager |
| Minimum:
? Demonstrated competency as a Novartis Clinical Research Associate.
? Thorough knowledge of Good Clinical Practices (GCPs), FDA Regulations and clinical trial monitoring practices.
? Excellent presentation and interpersonal skills.
? Excellent organization skills with the ability to prioritize and work effectively in a constantly changing environment.
? Strong written and verbal communication skills.
? Demonstrated ability to coach colleagues at various skill, knowledge and experience levels.
? Knowledge in computer technology and ability to support company use of electronic data systems including Electronic Data Capture.
? Ability to interact with a wide range of people and build strong, positive relationships with the CRA Group Head, DFM, Regional Associate Directors, Field Monitors and other training and development staff.
Preferred:
? Minimum five (5) years experience as a Novartis CRA with a degree in a scientific or health care discipline.
? Previous training experience.
? Working knowledge of Microsoft Office (e.g., Word and PowerPoint) and Lotus Notes. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| TS - Strategic Projects Leader |
| Ideal Background:
Education (minimum/desirable):
PhD, MD or PharmD level scientist or life science background with at least 5 years relevant experience. MBA is preferred.
Languages:
Fluent oral and written English
Experience/Professional requirement:
1. Strong knowledge of both early and late phases of pharma-ceutical drug development
2. Proven team leadership skills on complex projects
3. Ability deal with project start-up activities and implementa-tion
4. Excellent communicator ? good presentation and strong medical / scientific writing skills
5. Excellent team work in a multidisciplinary environment
6. Excellent organizational skills, as well as predisposition for innovation
7. Recognized for combining operational and scientific excel-lence in Drug Development |
| 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! |
| AstraZeneca Pharmaceuticals |
Boston |
MA |
11/19/2009
|
| Translational Strategist - Infection Research |
Degree level required and minimum years experience:
· A strong candidate would typically have a Ph.D. or M.D./Ph.D. and 10 or more years of experience, or equivalent experience, of which a minimum of 6 years should be in the pharmaceutical industry or other relevant setting
· Experience in anti-bacterial discovery and development is desirable
Competencies (knowledge and skills):
· Internally and externally recognized expertise in a scientific, technical or organizational area and the capacity to apply literature and theoretical concepts to the advancement of Infection portfolio goals.
· Possess strong problem solving skills and the ability to, on the basis of their own experience and analytical skills, ascertain the value of and initiate the use of new techniques for solving problems within and beyond their immediate project.
· Have a complete understanding of the AstraZeneca drug discovery and development process.
· Understand and work towards the AstraZeneca business objectives.
· Be highly productive: consistently generating high quality results within established time frames, even in areas of limited precedent.
· Possess strong knowledge and understanding of relevant database and scientific support software.
· Be a proactive communicator with excellent verbal and written communication and listening skills. Solicit opinions and feedback from others. Deliver presentations that are well thought out, informative and convincing. Able to present work at internal and external meetings when appropriate.
· Able to direct scientific staff and manage their performance.
· Able to effectively negotiate, persuade and influence others in a matrix environment.
· Capable of proposing and implementing scientific, technical or organizational ideas and initiatives.
· Able to manage multiple tasks efficiently, consistently generating high quality results within established time frames, even in areas of limited precedent.
Behaviors:
· Fosters environment of scientific excellence, innovation, productivity and timeliness, leading by example. Is reliable, has strong work ethic, and shows respect for colleagues
· Demonstrates leadership.
· Mentors and provides development opportunities for matrix or direct reports.
· Demonstrates commitment to team goals and consistently demonstrates influence in team & project meetings, advising project teams with respect to technical solutions and potential new approaches for consideration. Seeks solutions to issues that affect team morale and effectiveness
· Proactively shares expertise and ideas and is viewed as a resource by colleagues. Actively seeks to give advice and encouragement to the scientific community, promoting self as an approachable resource.
· Expands personal skills and knowledge as required to be effective. Demonstrates flexibility, open-mindedness, and adaptability. Projects creditability and professionalism. Is candid and honest in discussions
· Act in accordance with all AstraZeneca policies on personnel, SHE, best laboratory practice, etc.
 |
| Radiometer America, Inc. |
Dallas or Houston |
TX |
11/19/2009
|
| Transcutaneous Sales Specialist |
| •Bachelor’s degree in Science (i.e. Biology, Chemistry) or Nursing
•3+ years clinical experience in Respiratory Care, Hyperbaric/Wound Care Medicine or Cardiology
•3+ years medical capital sales experience
•Strong organizational, time management, territory planning skills
•Dynamic, high-energy individual to implement sales activities
•50% travel
If you are unable to apply electronically because of a disability, dial 711 to apply through the Ohio Relay and ask to be connected to the Human Resources Department at 440-871-8900.
Radiometer America Inc. is an equal opportunity / affirmative action employer and does not discriminate on the basis of race, color, gender, national origin, ancestry, religion, martial status, age, veteran status or disability or any other legally protected characteristics that may vary by state, city and/or county of employment.
|
| Morphotek®, Inc. |
Exton |
PA |
11/19/2009
|
| Training Administrator |
| Knowledge/Skills/Abilities Required
BA/BS in Business Administration, Human Resources, or a related field required.
2-3 years training, career counseling, career development or related experience in the biotechnology or pharmaceutical industry required.
Previous experience designing, delivering and/or implementing training programs required.
Experience in Learning Management Systems (LMS) and solid understanding of training operations required.
Advanced proficiency in MS Office applications required.
Excellent organizational, written communication, verbal communication, facilitation, presentation and interpersonal skills required.
Proven ability to work independently required.
Occasional travel may be required. |
| Johnson & Johnson Family of Companies |
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! |
| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| Therapeutic Brand Leader - Design for Launch ; Primary Care |
| Education:
- Advanced degree in science-related field, or other appropriate knowledge/experience (PharmD, PhD, MD)
Experience:
- >3 years managing programs in a team environment
- Strong knowledge of clinical development/operations
- Knowledge of development process and/or commercial strategies
- Ability to manage a diverse group of responsibilities
- Ability to work effectively in a cross-functional team environment
Skills and Competencies:
- Leadership abilities
- Expert technical depth in disease area
- Strategic influencing skills
- Highly developed written and verbal communication skills
- Well-developed initiative ability
- Excellent project management skills.
- Strong organization and time management skills.
- Strong analytical and problem solving skills.
- Knowledge of US business and brand operating models
- Scientific acumen
Preferred
- Minimum 5 years experience in a strategy-setting role within Medical Affairs
- Global experience within the pharmaceutical industry
- Working knowledge of FDA requirements
- Excellent computer skills (Excel, Word, Power Point, etc.)
- Knowledge of information/technology systems
- People management experience
- Negotiation skills
- Knowledge of MA organization
|
| Johnson & Johnson Family of Companies |
Glendora |
CA |
11/19/2009
|
| TEST LAB SUPERVISOR |
| Education and/or Experience: a Bachelors Degree in Electrical/Mechanical Engineering or related field with a minimum of 5 years industry experience and 3 years medical device experience. It is also required to have System Engineering experience in multi-disciplinary products ( Software and Hardware). Knowledge and experience in development processes and in documentation writing is an asset in this role. Lead, design, develop, and implement test equipment and test specifications is required.Strong knowledge of one or more of the following standards such as ASTM, UL, IEC 60601-1, ISO 8536-4 and ISO 10555-1 & -5 is preferred.Knowledge of GMP and other regulatory requirement is also preferred for this position.OTHER SKILLS and ABILITIES:Test Lab Supervisor will be expected to have strong analytical reasoning with excellent communication skills.Test Lab Supervisor will have the knowledge, skill and ability to provide technical support to project teams.If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Novartis Oncology |
na |
OH |
11/20/2009
|
| Territory Sales Manager - Toledo, OH |
| Minimum Education Required:
? Bachelor's degree or equivalent
Minimum Experience Required:
? 2-4 years successful outside sales experience
Preferred Level:
? One (1) year contact lens sales/opthalmic related sales/contact fitting experience.
Must have valid drivers license and the ability to travel extensively via automobile. Some air travel also required. Must successfully complete our ""New Hire Sales Training Program"". |
| Novartis Oncology |
na |
SD |
11/20/2009
|
| Territory Sales Manager - Sioux Falls, SD |
| Minimum Education Required:
? Bachelor's degree or equivalent
Minimum Experience Required:
? 2-4 years successful outside sales experience
Preferred Level:
? One (1) year contact lens sales/opthalmic related sales/contact fitting experience.
Must have valid drivers license and the ability to travel extensively via automobile. Some air travel also required. Must successfully complete our ""New Hire Sales Training Program"". |
| Novartis Oncology |
na |
OH |
11/20/2009
|
| Territory Sales Manager - Dallas, TX (East Dallas) |
| Minimum Education Required:
? Bachelor's degree or equivalent
Minimum Experience Required:
? 2-4 years successful outside sales experience
Preferred Level:
? One (1) year contact lens sales/opthalmic related sales/contact fitting experience.
Must have valid drivers license and the ability to travel extensively via automobile. Some air travel also required. Must successfully complete our ""New Hire Sales Training Program"". |
| Novartis Oncology |
na |
NY |
11/20/2009
|
| Territory Sales Manager - Brooklyn |
| Minimum Education Required:
? Bachelor's degree or equivalent
Minimum Experience Required:
? 2-4 years successful outside sales experience
Preferred Level:
? One (1) year contact lens sales/opthalmic related sales/contact fitting experience.
Must have valid drivers license and the ability to travel extensively via automobile. Some air travel also required. Must successfully complete our ""New Hire Sales Training Program"". |
| Novartis Oncology |
na |
NC |
11/20/2009
|
| Territory Associate |
| Bachelor?s Degree required.
1-2 years business to business sales experience desired.
50% travel within the United States/50% Greensboro, NC |
| 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 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
|
| 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 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 |
Cambridge |
MA |
11/19/2009
|
| Temporary Administrative Associate |
| H.S Diplmoa, A.A. or A.S. and 4-8 years relevant work experience, or B.A. (or equivalent degree) and 3-6 years of relevant work experience. Must have Lotus Notes experience.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Temp. Clinical Project Manager |
| PREFERRED EDUCATION AND EXPERIENCE:
M.S. (or equivalent experience) and 4+ years of relevant work experience
B.S. (or equivalent experience) and 6+ years of relevant work experience
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Temp. Clinical Project Manager |
| PREFERRED EDUCATION AND EXPERIENCE:
M.S. (or equivalent experience) and 4+ years of relevant work experience
B.S. (or equivalent experience) and 6+ years of relevant work experience
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company?s strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex?s product pipeline is focused on viral diseases, inflammation, autoimmune diseases, cancer, pain and bacterial infection. We are interested in establishing relationships with well qualified talent today for opportunities we plan to open in the future.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Temp. Admin Associate II |
| The associate should be comfortable with MS Word, Excel, Power Point and MUST BE proficient in Lotus Notes. The applicant should have 2-3 years of administrative experience and must demonstrate excellent skills in multitasking and problem solving. The individual will interface directly with other adminstrative associates in research and development, and the finance, travel and operations departments. Excellent communication and collaborative skills are a must.
Minimum scholastic requirements are a bachelors degree with 2-3 years of administrative experience and the necessary Apple computer literacy proficiency.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Temp QA Specialist |
| Bachelor's degree or equivalent in the Sciences. 5-7 years experience.
Vertex Pharmaceuticals |
| Novartis Oncology |
na |
NC |
11/20/2009
|
| Technician II, Lab |
| EDUCATION/EXPERIENCE:
High school diploma or equivalent required. Degree in physical sciences, statistics, or mathematics preferred. 3-5 years in a fast paced pharmaceutical environment and background in stability, statistics, chemistry or chemical analysis of pharmaceutical finished product dosage forms preferred. |
| Novartis Oncology |
na |
NC |
11/20/2009
|
| Technician II, HVAC |
| Education/Experience:
High School Diploma and 2 years of related experience; or Associate?s Degree or technical equivalent and no related experience. |
| Novartis Oncology |
na |
NC |
11/20/2009
|
| Technician II, Distribution |
| High School Diploma and 2 years related experience. Education: HS Diploma or equivalent required, some college preferred.
Work Experience: Proven commitment to customer service and a safe work environment. Must be team-oriented. Minimum 2-3 years of warehouse operational or manufacturing experience. Pharmaceutical experience is preferred, but not required. Strong attention to detail and accuracy. PC skills and inventory and shipping/receiving systems experience required; experience using SAP and Clippership preferred. Excellent communication (written and oral) and interpersonal (team building) skills. Minimum 2-3 years of fork-lift experience. |
| Biogen Idec, Inc. |
Cambridge |
MA |
11/20/2009
|
| Technician II, Animal Care |
â?¢ Minimum of 2-5 years directly related experience.
â?¢ AALAS certification is preferred or successful achievement of certification within 18 months of hire.
â?¢ Proficiency with basic technical procedures and identification methods.
â?¢ Good working knowledge of Microsoft Word and Excel.
â?¢ Strong organizational skills and attention to detail.
â?¢ Strong written and verbal English communication skills. Ability to follow written and verbal instructions.
â?¢ Ability to stand for extended periods of time.
â?¢ Ability to regularly lift/push, or pull up to 50 pounds.
Other
Regular work schedule is 40 hours per week; however, the incumbent may be required to work on weekends and holidays on a rotating basis. This position is over time eligible. |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Technical Writer IV |
| See above |
| BD (Becton, Dickinson and Company) |
Durham |
NC |
11/20/2009
|
| Technical Team Member- ADVANCED MOLDING SKILLS |
| See above |
| BD (Becton, Dickinson and Company) |
Durham |
NC |
11/20/2009
|
| Technical Team Member |
| See above |
| BD (Becton, Dickinson and Company) |
Durham |
NC |
11/20/2009
|
| Technical Team Member |
| See above |
| BD (Becton, Dickinson and Company) |
Durham |
NC |
11/20/2009
|
| Technical Team Member |
| See above |
| BD (Becton, Dickinson and Company) |
Durham |
NC |
11/20/2009
|
| Technical Team Member |
| See above |
| BD (Becton, Dickinson and Company) |
Durham |
NC |
11/20/2009
|
| Technical Team Member |
| See above |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Technical Support: Technical and Informatics Support Specialists (TAISS) |
| See above |
| Miltenyi Biotec Inc. |
Auburn |
CA |
11/20/2009
|
| Technical Support Scientist |
| Ph.D. in Immunology, Molecular Biology or similar field with 1-3 years experience in life sciences environment; or equivalent combination of education and experience. Flow cytometry experience is a must.
We offer a competitive salary and excellent benefits package. There is no relocation associated with this position. EOE/AA
To apply, go to: https://home.eease.com/recruit/?id=370281 |
| Miltenyi Biotec Inc. |
|
|
11/20/2009
|
| Technical Sales Consultant |
| Ph.D., M.S. or B.S. degree from a four-year college or university and two to four years experience in the life sciences environment; or equivalent combination of education and experience. Immunology and/or Molecular Biology background is preferred, and Ph.D. is highly desirable.
Other Requirements: Must possess a valid driver’s license, evidence of insurance / insurability and ability to receive appropriate clearance to access restricted government accounts.
We offer a competitive salary, commission, car allowance, and excellent benefits package. There is no relocation associated with this position. EOE/AA
To apply, go to: https://home.eease.com/recruit/?id=367955
|
| Novartis Oncology |
na |
CA |
11/20/2009
|
| Technical Manager CMO - Emeryville, CA |
| -Degree in related technical field (Biotechnology / Chemical Engineering / (Bio)chemistry) with doctorate (PhD) desirable or appropriate combination of education and experience.
-English fluent spoken and written; German & French spoken are a clear ?plus?
-Minimal 7-10 years confirmed experience in biotechnology manufacturing, ideally with direct responsibilities in manufacturing operations, 3rd-party management, toll-manufacturing activities or related area; Microbial expression system manufacturing background a plus. |
| 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 |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Technical Applications Specialist |
| See above |
| BD (Becton, Dickinson and Company) |
Wilson |
NC |
11/20/2009
|
| Tech Transfer Engineer |
| See above |
| Novartis Oncology |
na |
NC |
11/20/2009
|
| Tech Advisor I/Veterinary |
| Bachelor?s Degree in Scientific Field preferred
? Veterinary clinic experience preferred
? Previous scientific or medical background
? Knowledge of PC package tools including word processing (Word) and spreadsheets (Excel)
? Ability to effectively communicate verbally and in writing
? Ability to define problems, collect data, establish facts and draw valid conclusions
? Ability to interpret a variety of technical and scientific data
? Effective interpersonal skills
? Ability to work independently as well as a team member |
| Novartis Oncology |
na |
MN |
11/20/2009
|
| Team Leader, Target |
| ? BA/BS in Business Administration or related discipline; MBA preferred
? 10+ years combined sales experience
? 5 ? 10 years sales management experience including national accounts as well as internal head office rotation in category management and/or sale planning.
? Command of marketplace / account knowledge
? Working knowledge of marketing strategies & insights and ability to mobilize cross functional resources
? Exceptional communication, negotiation and motivational skills
? 25% Travel |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Team Leader, Customer Service |
| See above |
| BD (Becton, Dickinson and Company) |
Holdrege |
NE |
11/20/2009
|
| Team Leader |
| See above |
| 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 |
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 |
| Teva Pharmaceuticals USA |
North Wales |
PA |
11/20/2009
|
| Talent Development Specialist |
|
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Systems Consultant- Business |
| Principal Programmer
Responsible for all project level programming aspects (analysis datasets, pooled datasets, listings and tables) for drug project.
Major Activities:
1) Manage the programming activities for a global project following internal project management guidelines including resource planning.
2) Act as Program Programmer for assigned project and take a programming leadership role on the B & SR project team.
3) Maintain efficient interfaces with internal and external customers with advice from SR management.
4) Develop and comply with project/study standards and specifications following internal and regulatory guidelines.
5) Oversee programming style, quality of SR contributions and compliance with timelines.
6) Provide SR input and lead sections of Full Developments and Submission Working Groups.
7) Ensure the documents and specifications are consistent and comply with company standards by providing input into study protocol, CRF and data structures.
8) Program, according to specifications, analysis datasets, pooled datasets, listings summaries, figures and tables for Phase I-IV clinical trials and for SCS and SCE. Ensure quality control and quality audit of deliverables.
9) Maintain records for all assigned projects and archive trial/project analysis and associated documentation.
10) Participate in the selection of CROs, as required, and supervise SR project activities for CROs.
11) Train staff on trial and project level activities and internal processes.
12) Participate in or lead non-clinical project activities. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Systems Consultant - Business |
| Education :BA/BS or equivalent experience in mathematics, statistics computer science, life sciences or related field.
Languages: Fluent English (oral and written)
Experience/Professional requirements: (1) Expert knowledge of/experience with SAS software. (2) Good understanding of global clinical trials practices, procedures, methodologies.(3) Good understanding of regulatory requirements relevant to SR (e.g. GCP, ICH) (4) Experience in providing recommendations for maintenance or development of SR global policies, procedures and clinical data presentation standards. (5) Intermediate knowledge of office tools. (6) At least 8 years experience in a programming role preferably supporting clinical trials/ or in the pharmaceutical industry (5 years for MS Statistics/Computer Science graduates) |
| Vertex Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Systems Analyst-Enterprise Content Management |
| Preferred Education and Experience Levels
B.S and 5 years relevant work experience.
Knowledge/Skills Needed:
? Experience working in IT in regulated environments
? Must have excellent technical troubleshooting skills
? Good system analysis, design skills and familiar with SDLC methodology, particularly IQ, OQ, PQ
Technical
? Experience in ECM technologies such as Trackwise, QUMAS DocCompliance and Documentum (Content Server, eRoom)
? Experience in portal technology development and standards (JSR168, WSRP)
? Object-Oriented design skills: Java, JDK 1.4.x J2EE (JSP's, Servlet's, Tag Libraries) XML, XML Schema.
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain. Vertex co-discovered the HIV protease inhibitor, Lexiva, with GlaxoSmithKline.
Vertex Pharmaceuticals |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
11/20/2009
|
| System Project Engineer |
| See above |
| Agilent Technologies, Inc. US |
Columbia |
MD |
11/20/2009
|
| System Engineering Specialist |
| Qualifications:
?Bachelors or Master Degree or University Degree in Electrical/Electronic or Computer Engineering and 5+ years applicable experience in Mobile Communication Systems and Networks (including cell phone and other mobile communications infrastructure).
?Knowledge of UMTS, GPRS, GSM and CDMA technologies and Central Office networking.
?Experience with Perl and Shell Scripting as well as administration of Operating Systems: Linux and UNIX.
?Experience with end user, installation and commissioning of new systems within customer environments is highly desired.
?Strong interpersonal/relationship skills, solid written and verbal communications.
?US citizenship required
?Current US Government Security Clearance -or- ability to process for and obtain US Government Security Clearance.
Position will be located in northern Virginia or Maryland area. |
| Agilent Technologies, Inc. US |
Columbia |
MD |
11/20/2009
|
| System Architect |
| Qualifications:
Qualifications:
? Bachelors or Master Degree or University Degree in Electrical/Electronic or Computer Engineering and 5+ years applicable experience in architecting and implementing complex software solutions, and a deep understanding of Mobile Communication Systems and Networks. (Including Cell Phone and other Mobile Communications Infrastructure).
? Software project management, definition, development and deployment expertise.
? Understanding of the customers data streams and architecture where our products content will be used.
? Direct experience with SIGINT customers, products and applications.
? Experience in SIGINT acquisition systems, familiarity with content acquisition platforms in wireline, cellular telecom, and IP.
? End USER expertise in SIGINT missions
? Experience with end user, installation and commissioning of new systems within customer environments is highly desired.
? Familiarity with 7 layer OSI model and current and evolving telecoms standards including Wireless Protocols, with a strong background in IP
? Self starter and ability to self-learn
? Strong interpersonal/relationship skills, solid written and verbal communications
? US citizenship required.
? Current US Government Security Clearance -or- ability to process for and obtain US Government Security Clearance |
| 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! |
| BD (Becton, Dickinson and Company) |
Durham |
NC |
11/20/2009
|
| Support Technician |
| See above |
| BD (Becton, Dickinson and Company) |
Bedford |
MA |
11/20/2009
|
| Supply Network Planner |
| See above |
| 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. |
| 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
|
| 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. |
| Johnson & Johnson Family of Companies |
Memphis |
TN |
11/19/2009
|
| Supervisor, Operations - 3rd Shift |
| A minimum of a High School diploma is required. Bachelor's degree preferred. A minimum of 3 years of experience in Logistics, Operations or a related field is required. A minimum of 2 years of experience managing people, including conducting and delivering performance appraisals is also required. Experience in inventory management, including managing cycle counts, maintaining inventory records and performing inventory adjustments are preferred. Experience using Warehouse Management Systems (i.e. MARC Global) is preferred. Knowledge of Microsoft Office (Word, Excel, PowerPoint, Outlook) is required. Experience with Ariba Procurement System is preferred. Experience with Materials Resource Planning (MRP) Systems is preferred. Experience applying Six Sigma/Process Excellence Tools, Training and/or Certification preferred. Experience working in an Automated Distribution Center environment is preferred. An APICS certification is preferred. Knowledge of Service Level Agreement (SLA) requirements is preferred. Prior experience working in a real-time/fast-paced environment required. Must have strong leadership, interpersonal, analytical and organizational skills. Must have excellent collaboration, customer service and oral/written communication skills. Experience partnering with all levels of management in a cross-functional team environment is required. Must be able to work 3rd shift (11:00 pm - 7:30 am). The ability to work in a refrigerated environment at 2 to 8 C (35 to 46 F) for 2 hours or more at a time and in a freezer at -30 to -20 C (-4 to -22 F) for up to 1 hour at a time is required. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Biogen Idec, Inc. |
Cambridge |
NC |
11/20/2009
|
| Supervisor, Manufacturing |
Must have Excellent GMP documentation skills. A Full understanding of bio-processing (Purification, Cell Culture, Dispensing operations, and Production support)
A Fundamental knowledge of validation is required. Must have good troubleshooting skills. Strong interpersonal, leadership and communication skills are required. |
| Biogen Idec, Inc. |
Cambridge |
MA |
11/20/2009
|
| Supervisor, Animal Facility |
â?¢Minimum of six to eight years directly related laboratory animal experience with at least three years supervisory experience
â?¢Certification/Licensure: AALAS certification at the LATG level, and CVT certification is preferred
â?¢Knowledge and experience of animal husbandry and sanitization requirements, and cagewash operations
â?¢Knowledge and experience in proper methods of small laboratory animal husbandry, handling and restraint, injection and sample collection techniques and euthanasia procedures
â?¢Advanced understanding of colony health status requirements and applicable animal care regulations
â?¢Excellent interpersonal, supervisory, and leadership skills. Demonstrated ability to interact professionally with investigators, contractors, vendors, and staff
â?¢Sound judgment and decision making skills, effective written and verbal communication and supervision skills
â?¢Excellent organizational and observational skills
â?¢Ability to work independently with minimal supervision
â?¢Advanced working knowledge of Microsoft Word and Excel
â?¢Ability to lift, push/pull 50 pounds |
| BD (Becton, Dickinson and Company) |
Columbus |
NE |
11/20/2009
|
| Summer Engineering Internship |
| See above |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Study Support Associate II |
| BS/MS in biomedical science, pharmacology, or related discipline. Hands-on experience with animal models is essential, and the selected candidate should also have experience in virology and/or bacteriology is preferable. An understanding of pharmacokinetics is desirable. The candidate should also have experience in experimental design, animal surgery, microbiology techniques, data interpretation, and statistical analysis. A strong work ethic, excellent oral and written communication skills, and the ability to function in an interdisciplinary team are essential. |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Strategic Sourcing Manager - Professional Services & Manufacturing |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Strategic Sourcing Manager - Indirect Services |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Strategic Sourcing Manager |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Strategic Sourcing Analyst |
| See above |
| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| Strategic Project Mgr |
| Minimum Requirements:
5-7 years of commercial pharmaceutical industry experience
Minimum of 3 years of project management experience.
Exceptional interpersonal, communication, leadership, and facilitation skills
Demonstrated proficiency in all Microsoft applications
Bachelor?s degree in Business, Business Administration, Marketing, Communication, Organizational Design, Human Performance, or other relevant discipline
Preferred Background:
- Pharmaceutical Marketing, Marketing Research, Change Management, or other relevant Commercial experience
- 5+ years of strategic/process/change management business consulting experience
- Demonstrated ability to lead and produce results in a matrix environment: ?Lead without Authority?
|
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Strategic Procurement Project Manager |
| ? Degree or equivalent with a background and experience in business, finance or similar
? Strong communication, analytical and administrative capabilities
? Strong and creative IT skills; must have advanced Excel skills
? Experience in pharmaceutical/generics industry within Supply Chain or Purchasing
? Knowledge of data management & reporting
? Exposure to or experience in Knowledge management
? Exposure to or experience in E-Auctions, procurement practise. |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Strategic Marketing Manager |
| See above |
| 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. |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Strategic Innovation Leader |
| See above |
| Vertex Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Stock Plan Administrator |
| Minimum Education Requirements:
Bachelor's Degree and at least 2-3 years of experience as a stock plan administrator experience.
Required experience and/or qualifications:
This individual will have excellent communication skills and the ability work with departments and employees with varying levels of knowledge. In addition this individual must have a proven ability to manage time lines and deliverables. The ideal candidate will display advanced knowledge of equity administration, applicable rules and regulations, industry standards, industry practice. The ideal candidate will have an in- depth working knowledge of the Equity Edge database. Must have knowledge and experience using Equity Edge application. CEP, a plus.
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain. Vertex co-discovered the HIV protease inhibitor, Lexiva, with GlaxoSmithKline
Vertex Pharmaceuticals |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Statistician II - Shanghai China |
| ? At least Master?s Degree in statistics or a closely related field.
? At least 2 year of experience in drug development (maybe acquired at a CRO) or a related area (no prior work experience required for Ph.D.).
? Good communication skills, including ability to communicate in English verbally and in writing.
? Ability to give effective guidance to programmers.
? Knowledge of and experience in using statistical software, in particular SAS
Work Location: Shanghai, China |
| 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! |
| Teva Pharmaceuticals USA |
North Wales |
PA |
11/20/2009
|
| Staffing Partner |
|
| 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! |
| 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. |
| Johnson & Johnson Family of Companies |
|
CA |
11/19/2009
|
| Staff Quality Engineer - Irwindale, CA |
| A minimum of a Bachelor's degree in Engineering, Physical, Biological, or natural sciences, along with a minimum of 8+ years of quality, manufacturing, or research and development experience in a medical device or other regulated industry is required. An MBA, Master's, or advanced degree in an applicable field of study is an asset. An American Society for Quality (ASQ) certification is an asset. Experience or knowledge of Six Sigma, Lean Manufacturing, or Process Excellence tools is desirable. Must have the ability to use broad knowledge of regulatory, technical, and business requirements to conduct due diligence assessments. Project management experience or skills ensuring fulfillment of new product development requirements is required. Development and implementation of Quality standards applicable to the medical device or other highly regulated industry required. Knowledge of Quality and Operations systems and processes, including GMP, in a regulated industry is required. A knowledge of Quality Systems Regulations (QSR) requirements as they relate to medical devices is required. Auditing experience is an asset. Knowledge of Quality Engineering, design control, and verification and validation (V&V) tools and methodologies required. The ability to effectively communicate with internal and external personnel at all levels of the organization will be needed. Well-developed influencing and negotiation skills and the ability to effectively train and mentor a diverse array of employees at all levels of the organization will be needed. Business and financial acumen 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! Due to technical upgrades, this requisition is replacing requisition # 0903032. Any candidates who have already applied to requisition # 0903032 are already being considered, therefore, you do not need to apply. |
| Johnson & Johnson Family of Companies |
|
CA |
11/19/2009
|
| Staff Process Engineer |
| A minimum of a Bachelor's degree and a minimum of 9 years of engineering related experience OR a Masters degree and a minimum of 7 years of engineering related experience OR a Ph.D. and a minimum of 4 years of engineering related experience is required. Complex understanding of polymer and engineering fundamentals is required. Experience in a highly regulated industry is required. Experience in the medical device or pharmaceutical industry is an asset. A clear mastery of statistical and experimental engineering techniques is required. Proficiency with Microsoft Office, specifically Excel is required. Experience with Microsoft Project is preferred. Experience with balloon catheter process and polymer bonding is preferred. Experience with Six Sigma/Process Excellence Tools, Training, and/or Certification is preferred. Experience managing complex projects is required. Excellent verbal and written communication skills are required. This candidate will have strong analytical/problem solving skills. Ability to work on cross functional teams is required. The ability to develop and lead teams, strong collaborative skills, and the ability to negotiate and influence are required. This position will require that you be based in Menlo Park, CA and travel 10% of the time internationally and domestically. 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 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! |
| 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. |
| 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 |
|
CA |
11/19/2009
|
| Staff Engineer- FEA Analyst |
| EDUCATION and/or EXPERIENCE: MS in Engineering Mechanics (or related engineering discipline) and three or more years of related engineering experience; or Ph.D. in Engineering Mechanics (or related engineering discipline). Experience with ABAQUS IMPLICIT and/or EXPLICIT software in an industrial setting is strongly preferred.. Experience with Statistical Analysis, Metal Plasticity and Metallurgical Principles is preferable. Experience with using LINUX or UNIX operating systems is strongly preferred. Experience with CAD software is also strongly preferred. Experience in the medical device industry would be an asset. Other skills and abilities include: A clear mastery of theoretical and mechanics principals is required for this position and experience with experimental engineering techniques is an asset. English communication skills, written and oral 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! |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Staff Engineer, Packaging Technology |
| See above |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Staff Engineer - Sterile Process/Capital Project Support |
| Requirements:Bachelor of Science in Chemical Engineering, Mechanical Engineering, or Biomedical Engineering 2 years experience in a process engineering support or capital project engineering role supporting an FDA regulated process Preferred:Experience with a sterile/aseptic process Experience with a pharmaceutical manufacturing process Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition #CHE002165. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Staff Engineer - Protein Purification |
| Required:Bachelors degree in Engineering or Science Discipline 2 years experience in a GMP regulated environment with some or all of that time spent in an Engineering role in support of a process that includes protein purification (will consider a Master's degree in Chemical Engineering, BioChemical Engineering or Biomedical Engineering in lieu of experience) Preferred:Experience with a facility start up Experience with validation qualifications for a start up facility Engineering support experience with a vaccine product Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition #CHE002144. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| 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! |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Staff Engineer - Fermentation Process Support |
| Required:Bachelor degree in Engineering or Science field 2 years experience in an engineering or operations position supporting a manufacturing process through one or more of the following roles: process improvements, monitoring process performance, investigating atypicals and implementing corrective actions, creating standard work for operations, and assisting in troubleshooting of the process. Preferred:Experience with technical support of a GMP (good manufacturing practices) manufacturing process BS degree in Chemical Engineering, Biotechnology, Chemistry/Biochemistry Experience in bioprocess manufacturing Experience with fermentation and/or purification processes for production of proteins Supervisory experience Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # CHE002156. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Staff Engineer - Environmental Sustainability |
| See above |
| 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. |
| Johnson & Johnson Family of Companies |
Cincinnati |
OH |
11/19/2009
|
| STAFF DESIGN ENGINEER - ELECTRICAL |
| BS degree in electrical engineering, or related field is required. MS degree is preferred. At least 8 years of experience in the planning, design, and commercialization of electrical or electro-mechanical systems, including embedded software is required. The ideal candidate will have a demonstrated track record of driving technically appropriate solutions and the effective use of new technology. DFSS or similar certifications preferred. Medical products or other highly regulated industry is an asset. Technical leadership and project management, particularly with globally outsourced projects is an asset. RF Analog products with experience in design, test and interconnecting/cabling is a requirement for this role. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Staff Chemical Engineer |
| This position requires candidate to be currently enrolled in a MS program in Chemical Engineering, Biochemical Engineering, BioMedical Engineering (process option), Bioengineering, or related field. Ideal candidate will possess superior communication and interpersonal skills. Must be graduating between August 2009 and August 2010. Candidates must be eligible to work in the US without sponsorship. Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # CHE002019. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
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. |
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. |
| Vertex Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Stability Manager |
| A Bachelor's Degree and 8 year of Quality Control experience with emphasis on stability program management or equivalent is needed.
Required experience and/or qualifications:
? Management of complex projects
? Working knowledge of trend analysis software is necessary.
? Thorough understanding of cGMP and ICH guidelines
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company?s strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex?s product pipeline is focused on viral diseases, inflammation, autoimmune diseases, cancer, pain and bacterial infection.
Vertex Pharmaceuticals |
| 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 |
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! |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Sr.Regulatory CMC Liaison Manager |
| Education and/or Professional Experience:
Degree in Science (e.g. Chemistry, Pharmacy, Biochemistry, Biotechnology, Biology) or equivalent.
Desirable:
Advanced degree in Science (e.g. Chemistry, Pharmacy, Biochemistry, Biotechnology, Biology) or equivalent.
Languages:
Fluent English required (oral & written). Good skills in site (local) language desired (oral).
Experience/Professional Requirements:
6-8 years in regulatory preferred, and/or experience in drug/biologic pharmaceuticals
Working knowledge/experience in regulatory submission and approval processes for New Chemical Entities (NCE) and product life cycle management and proven practical knowledge of and ability to deal with complex CMC regulatory issues and requirements.
Proven track record of successfully working in interdisciplinary teams, and of planning, coordinating and leading activities simultaneously on multiple projects.
Regularly demonstrated active contributions to line functions or project teams, as well as ability to contribute to matrix teams with the necessary strategic thinking.
Demonstrated ability for strategic thinking, maintaining awareness of business impact.
Demonstrated ability for risk assessment and mitigation.
Computer literacy (e.g. MS-project, Power Point, document management systems) available and shown ability to quickly learn new software and tracking tools and associated processes.
Strong interpersonal, communication, negotiation and problem solving skills. |
| Agilent Technologies, Inc. US |
Columbia |
MD |
11/20/2009
|
| Sr. Systems Design Engineer |
| The position requires a BSEE/MSEE with emphasis in digital signal processing (DSP). Must have proven ability to use computer tools for simulation, coding and measurement (i.e. MatLab) and working knowledge of C and/or C++ languages within Microsoft Windows? and Linux operating system frameworks. Ability and desire to work on rapid paced projects with several design tasks. Ability to work effectively as a member of a geographically dispersed team of engineers both in our core labs and in other functional areas including our sales group. Chosen candidate must have excellent communication skills, both verbal and written. Must be willing to travel when necessary.
? Must be a US Citizen
? High-level government security clearance is required
Desired Skills:
? MSEE with emphasis in communications signal analysis and processing
? In-depth knowledge of programming with Visual Studio? and Wind River DIAB development environments
? Experience in design of demodulators including digital PLL's, digital filters and bit coding/decoding algorithms
? In-depth knowledge of complex receiver and signal processing chains
? Working knowledge of the Agilent E3238s system
? Knowledge of measurement techniques and considerations in the wireless market
? Working knowledge of direction finding |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Sr. Systems Analyst - Logistics Execution |
| See above |
| Vertex Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Sr. Systems Analyst |
| Necessary technical skills:
? Experience implementing and supporting proven middleware technologies.
? Languages: SQL, PL/SQL, scripting languages
? Databases: Oracle 10g
? OS: Unix, Linux, Windows
? ETL Tools: Data Loader, SQL*Loader
? Use of API?s in data processing following coding standards
Preferred technical skills (a plus):
? Applications: Oracle E-Business Suite11 i (11.5.10.2), specifically Oracle Process Manufacturing and Oracle supply chain modules
? Developer Tools: Oracle Developer Forms, Oracle Developer Reports, Oracle Discoverer (9i, 10g), Oracle Alerts, Oracle Workflow builder, BI Publisher (XML Publisher), Web ADI
Technical and Communication Skills:
? Ability and desire to learn quickly and in a self-paced environment
? Hands on experience with Oracle 11.5.10 HR, OPM, and Supply Chain Management
? Ability to work within a fast-paced small team to deliver quality results
? Ability to work interactively with users, management and support team.
? Team contributor with good communication skills and strong analytical, problem solving skills.
? Expertise in Oracle 11.5.10 financials modules like Oracle General Ledger, Oracle Payables, Oracle Assets, Oracle purchasing, Cash Management, Project Accounting is a plus
Preferred Education and Experience Levels:
? B.S and 5 years relevant work experience.
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain. Vertex co-discovered the HIV protease inhibitor, Lexiva, with GlaxoSmithKline
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Sr. Staffing Consultant - Customers & Markets |
| - Minimum of 6+ years corporate pharmaceutical sales and commercial recruiting experience, or equivalent, working in a fast-paced matrix organization. Experience in building a pharmaceutical field force from the ground up highly preferred
- Proven track record in finding unique ways of sourcing qualified candidates, cold calling, relationship building and networking, resulting in successful placements of premium talent. Those individuals with a strong network in this area (Sales/C&M) are urged to apply
- Superior selection skills and proficiency in assessing individuals and small teams, in particular having extensive experience in successfully screening and assessing sales professionals
- Knowledge and experience with staffing and sourcing technologies and adherence to established policies and procedures
- Proven ability to develop successful relationships with business partners, staffing team members and entire HR team
- Demonstrated listening, facilitation and communications skills
- Ability to travel for recruitment and networking events
- Ability to work in a fast-paced, changing environment. We are growing rapidly and change is the constant so bring a positive can do attitude
- Results driven, able to demonstrate/quantify success relative to established targets and metrics
- Experienced and political savvy working with different levels within an organization
- Applicants must possess strong organizational, computer and web skills, along with the ability to multi-task and handle sensitive and confidential situations/information
- Ability to demonstrate Vertex?s core values on a day to day basis when working collaboratively with internal and external individuals as well as when building strategy, and executing tasks or initiatives
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain. Vertex co-discovered the HIV protease inhibitor, Lexiva, with GlaxoSmithKline.
Vertex Pharmaceuticals |
| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| Sr. Staff Veterinarian |
| Minimum Requirements
?DVM (or equivalent) and licensed to practice in the US or equivalent
?License to practice in at least one state in the United States
?ACLAM board certification or board eligibility
?1 to 5 years of laboratory animal medicine experience, with record of increased responsibilities and accomplishments, in either a pharmaceutical or academic environment
?Knowledge of regulatory requirements for the care and use of animals in research
?Experience working in a matrixed multidisciplinary environment and knowledge of the drug discovery and development process
?Effective communication, organizational and technical skills
?Strong interpersonal skills with an ability to collaborate and work in teams
?Ability to motivate others, positively influence people, and work in a team environment
|
| 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. |
| Morphotek®, Inc. |
Exton |
PA |
11/19/2009
|
| Sr. Scientist - Pharmacology |
| Job Requirements and Qualifications
Education: PhD with training in pathology, cell biology or related fields, expertise in oncology preferred but not required.
Must have at least 5 years experience in biotech/pharmaceutical industry.
Strong experimental skills in human disease model development, mammalian tissue culture, vector transduction and imaging-related technology.
Oncology experience is preferred. Experience in IHC is a plus.
A thorough understanding of molecular oncology and immunology.
Demonstrated experience in in vivo human disease model and an excellent publication record.
Supervisory experience preferred.
Excellent organizational, time management, communication, and interpersonal skills.
Strong oral and written skills, and experience maintaining a record of studies in the form of notebooks, technical reports, summaries, protocols, and quantitative analyses.
Other Information
Special Information (Travel required, physical requirements, on-call schedules, and etc.):
Some travel may be required.
|
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Sr. Programming Specialist |
| Education: BA/BS or equivalent experience in mathematics, statistics, computer science or life sciences or related field.
Languages: Fluent English (oral and written)
Experience/Professional requirement:: (1) Intermediate knowledge of /experience with SAS software. (2) Working knowledge of database. (3) Good understanding of global clinical trial practices, procedures, methodologies. (4) Good understanding of regulatory requirements relevant to SR (e.g. GCP, ICHP (5) Intermediate knowledge of MS Office tools. (6) At least 4 years experience in a programming role preferably supporting clinical trials/or in the pharmaceutical industry (2 years for MS Statistics/Computer Science graduates). |
| 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 |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Sr. Product Manager |
| See above |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Sr. Principal Biostatistician |
| Education Minimum/desirable): At least Masters Degree in Statistics (or equivalent degree with 6 years of experience or PhD with 2 years of experience.
Languages: Fluent English (oral or written).
Experience/Professional requirement:
1. Experience in all tasks of a Trial Statistician.
2. Proven knowledge in Statistics and its applications to clinical trials.
3. Proven knowledge of drug development and HA guidelines. Background medical knowledge preferably in relation to the specfic therapeutic area.
4. Proven knowledge of statistical software packages.
5. Good communication and presentation skills.
6. Good team player. |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
11/20/2009
|
| Sr. Packaging Engineer |
| See above |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Sr. Oncology Director Clinical Research Physician |
| MD required. Board certified hematologist/oncologist preferred. Advanced knowledge of oncology required. Must have >5 years of demonstrated leadership and accomplishment in clinical trials and/or medical affairs (planning, executing, reporting clinical trials, leading medical affairs activities) in academia/pharmaceutical industry. People management experience and matrix management experience required. Strong leadership, management, interpersonal, communication, negotiation, and problem-solving skills. Ability to think strategically. Organizational awareness (inter-relationship of departments, business priorities), and experience working on cross functional teams desired. Excellent written and oral communication skills, including presentation skills. Fluent oral and written English. Ability to interact effectively with external customers and internal stakeholders. Ability to travel, US and International. |
| Vertex Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Sr. Medical Writer |
| Ph.D. (or equivalent degree) and 2 ? 5 years of relevant work experience, or M.S. (or equivalent degree) and 3 ? 6 years of relevant work experience, or B.S. (or equivalent degree) and 4 ? 8 years of relevant work experience
Vertex Pharmaceuticals |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Sr. Manufacturing Equipment Engineer - Reagents |
| See above |
| Astellas Pharma, Inc. |
Deerfield |
IL |
11/19/2009
|
| Sr. Manager/Assistant Director, CMC |
| ? A M.S. or Ph.D. in Pharmacy, Pharmaceutics, life sciences or Chemistry plus 3-5 years of experience in the pharmaceutical development of investigational drug candidates is required. A B.S. in Pharmacy or Chemistry with additional relevant experience (5-10 years) can be considered. Title and grade will be based degree and experience as well as the degree of fitness to the Essential Job Responsibilities? Experience with multiple aspects of the process development, analytical characterization, process scale-up and/or regulatory registration of biotechnology drug substances proteins or peptides) is required. ? A thorough knowledge of current pharmaceutical and related industry and processes and practices, and the ability to leverage this knowledge to optimize group and departmental processes is essential.? Experience in the management of contract research organizations or collaboration partners is preferred.? Excellent communication and project management skills are required as this position is responsible for the scientific evaluation and coordination of work performed by external organizations. ? The ability to manage multiple projects and to work well within a team environment are also essential. ? An working understanding of GMP requirements and FDA/ICH guidance is required, as well as facility with commonly available computer tools for project management and data evaluation. |
| Millennium Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Sr. Manager, Regulatory CMC |
|
| Teva Pharmaceuticals USA |
North Wales |
PA |
11/20/2009
|
| Sr. Manager, Network Administration & IT Security |
|
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Sr. Manager, IT Comm Ops |
| Education:
Bachelor?s degree in Information Technology or related field. Masters degree preferred.
Project Management certification
Experience:
Minimum 8 years of IT experience
Prior experience of IT operational management and team leadership
Experience in the US Pharmaceutical industry is required ? experience in the generics industry would be an advantage
Significant IT project management experience
Knowledge of SOX and GxP compliance |
| Millennium Pharmaceuticals |
Boston |
MA |
11/19/2009
|
| Sr. Manager, Clinical Operations |
|
| Astellas Pharma, Inc. |
Deerfield |
IL |
11/19/2009
|
| Sr. Manager Procure to Pay |
| REQUIREMENTS:- BS/BA in Accounting, MBA preferred- Strong knowledge of business processes- Strong knowledge of Financial IT systems- Public accounting experience preferred- Understanding of US Sarbanes-Oxley and on-going compliance requirements.- Expertise in evaluating and implementing process-level business processes- 7+ years working experience in accounting.- 2+ years management experience - Strong verbal and written communication skills a must. |
| Millennium Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Sr. Manager / Assoc Director, Clinical Supply Operations |
|
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Sr. Financial Analyst - Finance Leadership Development Program (2 of 2) |
| See above |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Sr. Engineer/Scientist - Manufacturing Process Technical Support |
| Minimum Qualifications: Bachelor's degree in Chemical, BioChemical or Bioprocess Engineering with 5 years experience in a GMP Biopharmaceutical manufacturing or research and development environment OR Master's degree in Chemical, BioChemical or Bioprocess Engineering with 2 years experience in a GMP Biopharmaceutical manufacturing or research and development environment Preferred Qualifications:Experience providing technical support of a GMP manufacturing process, specifically in protein purification and/or fermentation. Experience writing technical documentation: such as change controls, protocols, operating procedures. Experience with commissioning, qualification, and validation of biopharmaceutical equipment and processes. Demonstrated expertise in bioprocessing unit operations such as fermentation, chromatography, tangential flow filtration Demonstrated ability to lead a group of individuals in task oriented assignments such as technical investigations, root cause analysis, equipment installation Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. We offer an excellent salary and an industry-ranked benefits program, including tuition reimbursement, work-life balance initiatives and developmental programs at all levels. Merck's retirement package includes a pension plan and one of the best 401(k) plans in the nation. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # CHE002082. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Our work is someone's hope. Join us.Where patients come first - Merck Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Sr. Engineer - Sterile Process/Capital Project Support |
| Requirements:Bachelor of Science in Chemical Engineering, Mechanical Engineering, or Biomedical Engineering5 years experience in a process engineering support or capital project engineering role supporting an FDA regulated processPreferred:Experience with a sterile/aseptic processExperience with a pharmaceutical manufacturing process Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. We offer an excellent salary and an industry-ranked benefits program, including tuition reimbursement, work-life balance initiatives and developmental programs at all levels. Merck's retirement package includes a pension plan and one of the best 401(k) plans in the nation. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition #CHE002167. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Our work is someone's hope. Join us.Where patients come first - Merck Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Sr. Engineer - Protein Purification |
| Required:Bachelors degree in Engineering or Science Discipline 5 years experience in a GMP regulated environment with some or all of that time spent in an Engineering role in support of a process that includes protein purification Preferred:Experience with a facility start up Experience with validation qualifications for a start up facility Engineering support experience with a vaccine product Our employees are the key to our company's success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program. Merck's benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition #CHE002143. Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| BD (Becton, Dickinson and Company) |
Sandy |
UT |
11/20/2009
|
| Sr. Electro-Mechanic |
| See above |
| Astellas Pharma, Inc. |
Deerfield |
IL |
11/19/2009
|
| Sr. Director, Oncology Global Strategic Marketing, Product & Portfolio Strategy |
| ? Minimum 7-10 years of pharmaceutical/life sciences experience in, preferably, a strategic marketing, new product development, business development, or similar role? MBA or advanced science degree ? Oncology commercial experience? Global commercial experience? Previous co-promotion experience ? In-depth understanding of the clinical development process |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Sr. Demand Planner |
| - The individual should have 2-4 years of product sales forecasting/ demand planning experience. Previous experience in consumer products a plus
- The position requires the individual to be exceptionally detail oriented and well organized.
- Exposure to SAP APO forecasting module, familiarity with DRP planning systems, IRI and a Business Intelligence (BI) reporting tool required
- The individual must have strong analytical, interpersonal and communication skills
- Ability to handle and understand large amount of data and communicate demand to various levels of organization
- Bachelors Degree required |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Sr. Data Manager |
| Education: Bachelors degree in life sciences, computer science, pharmacy, nursing or equivalent relevant degrees.
Languages: Fluent English (oral and written)
Experience/ Professional Requirements:
1) Ideally 5 or more years experience in drug development with at least 4 years in Data Management activities.
2) Project team leadership experience required.
3) Good technical and problem solving skills.
4) Thorough understanding of clinical trial methodology GCP and medical technology.
5) Ability to work independently, under pressure demonstrating initiative and flexibility.
6) Attention to detail and quality focused.
7) Good organization planning and project management skills.
8) Good interpersonal and communication skills and ability to operate effectively in an international environment.
9) Good negotiation skills.
10) Thorough understanding of physiology, pharmacology, clinical study objectives and the drug development process.
11) Ability to mentor, coach within Data Management and cross functionally and train internal and external partners. |
| BD (Becton, Dickinson and Company) |
Sumter |
SC |
11/20/2009
|
| Sr. Cost Analyst |
| See above |
| Biogen Idec, Inc. |
Cambridge |
MA |
11/20/2009
|
| Sr. Compensation Analyst |
â?¢ Experience (5-7 years) in compensation design and analysis with strong quantitative and analytical skills.
â?¢ Preferred background will include consulting firm experience, biotech/pharma sector experience and experience in a commercial (sales and marketing) organization.
â?¢ Proven critical thinking capabilities, judgment, ethical standards and interpersonal communication skills are required.
â?¢ Ability to effectively prioritize, take initiative and consistently deliver high-quality, accurate work within deadlines is required.
â?¢ Advanced capabilities in analysis and modeling with MS-Excel and other analytic tools is required. |
| 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! |
| 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. |
| Novartis Oncology |
na |
CA |
11/20/2009
|
| Sr Technical Project Leader - Vacaville, CA |
| Advanced degree in scientific or relevant discipline or equivalent
Desirable: Ph.D. in scientific or relevant discipline or equivalent
Additional requirements:
Excellent English required (oral & written). Good skills in site (local) language desired (oral).
?Demonstrated 5 ? 10 years of successful performance in the role of leading interdisciplinary teams of scientists working on technical projects within TECHNICAL Line Functions or equivalent experience in line function management or from external company.
?Proven track record as actively contributing Technical Project Team Representative or Project Team Member in IPTs / FIPs for a number of projects within the Novartis group or equivalent experience.
?Demonstrated ability to successfully manage budget(s), resources and associated development plans of assigned projects with adequate proactive planning and communication to involved functions or equivalent experience from line function management (e.g. section budget).
?Proven track record in coaching associates within technical line functions or adequate experience from line function management or external company.
?Significant further professional development such as scientific expertise and understanding in the required areas, advanced and continuous education in project management methodologies and basic commercial principles. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Sr Submissions Coordinator |
| Education:Minimum: bachelors degree with experience equivalent to graduate degree
Desirable: University degree (Diploma, Masters or Doctoral in life sciences, chemistry, business admin)
Languages:English fluent (oral and written)
Experience/Professional requirement:
? 3 years experience in Clinical Pharmacology, or Toxicology, or Preclinical Safety, or in any other TS discipline
? Advanced knowledge of CTD requirements
? Advanced knowledge of internal submission requirements and external regulatory requirements.
? Advanced knowledge of CREDI and PREDI
? Advanced knowledge of GXPs
? Prior submission experience
? Ability to lead multidisciplinary teams
? Advanced knowledge in all aspects of drug development
? Excellent oral and written communication skills
? Advanced knowledge of regulatory requirements and pharmaceutical development
? Working knowledge and compliance with the Good Laboratory Practices and Standard Operating Procedures
? Excellent organizational skills and advanced team-work skills with customer focus emphasis.
? Strong willingness and aptitude for learning and adapting new information and innovations |
| Millennium Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Sr Software Engineer, Cognos Reporting |
|
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Sr Scientist, Clinical PK/PD |
| Minimum Requirements:
Ph.D. level scientist with biological background with at least 0-2 years experience in drug development or a relevant environment (e.g. Clinical Pharmacology, Drug Metabolism and Pharmacokinetics).
In depth knowledge of PK and PK/PD evaluation techniques required.
Experience of working in a team environment a plus.
Knowledge of regulatory requirements and experience in dealing with regulatory authorities either through written summaries or oral presentations is desired, but not essential.
The individual must be very effective at technical and scientific problem solving in a project driven, multi-disciplinary international environment, able to focus and work on several projects simultaneously and must posses excellent interpersonal, leadership and teamwork skills with very good organizational skills (e.g. planning and time management).
Must be fluent in written and spoken English. |
| Vertex Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Sr Scientist, Chemical Development |
| - A Ph.D. degree with 6+ years of current and relevant academic, post-doctoral, or industrial process chemistry experience; an MS degree with 7+ years of industrial process chemistry experience; or a BS degree with 10+ years of industrial process chemistry experience. Degrees should have a life science focus with a preference for a concentration in Chemistry, Organic Chemistry, Process Chemistry or Medicinal Chemistry
- The proven ability to successfully interact, lead, and collaborate within an interdisciplinary team environment comprised of organic, physical, and analytical chemists; chemical engineers, project team members; and manufacturing personnel
- A track record of innovation, self-starting and success working in a multi-disciplinary team under defined timelines
- Experience operating under GMP guidelines with a preference for a working knowledge of quality principals
- Working knowledge of NMR and HPLC
- Experience interacting with contract research (CRO) and contract manufacturing (CMO) organizations
- The ability to communicate ideas across an organization through effective verbal and written communication skills
Although Vertex does not have an active opening, we are interested in establishing relationships with well qualified and talented individuals for future opportunities in our Chemical Development group in Cambridge, MA.
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company?s strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex?s product pipeline is focused on viral diseases, inflammation, autoimmune diseases, cancer, pain and bacterial infection.
Vertex Pharmaceuticals |
| Novartis Oncology |
na |
NE |
11/20/2009
|
| Sr Scientist II |
| Degree(s) in chemistry or related disciplines. Typically requires minimum education and experience as follows:
Ph.D. with 2-6 years relevant experience, MS with 6+ years or BS with 8+ years.
? Thorough knowledge of chemical principles; Excellent analytical skills; Excellent written and communication skills; Thorough experience in analytical instrumentation, GMPs, and validation of analytical procedures; Should be creative and show initiative. |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Sr Scientist |
| See above |
| Vertex Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Sr Scientific Associate, Analytical Development |
| - A Master's or Bachelor's degree in the life sciences or physical sciences with a preference for a concentration in Chemistry, Analytical Chemistry or Pharmaceutical Chemistry
- 0 - 4 years of academic experience in a chemistry or analytical chemistry laboratory setting with some previous related industry experience preferred
- Familiarity with, or a desire to gain a working understanding of, HPLC, LC-MS, GC, GC-MS, FT-IR, UV-VIS, KF and other instruments used in the analysis of pharmaceutical products
- An interest in and passion for establishing a career in analytical development and the biopharmaceutical industries
- The ability to work successfully in both a team environment as well as independently
- Excellent written and verbal communication skills
- Established organizational skills
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain. Vertex co-discovered the HIV protease inhibitor, Lexiva, with GlaxoSmithKline.
Vertex Pharmaceuticals |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Sr Safety Assessment Expert |
| PhD in pharmacology, toxicology or a related biological science; MD with appropriate experience, DVM with appropriate training and experience. PharmD or equivalent with a strong biological background or equivalent work experience.
Languages: Fluent English (oral and written).
Experience/Professional requirement:
1. Level-dependent.
o Base level: At least 2 years experience as a part-time safety assessment project team representative alongside other duties such as study director; experience with biologicals safety assessment desirable.
o Senior level: At least 3 years experience as a full time safety assessment project team representative, preferably with a mix of research, exploratory development and full development teams including experience of biological products
o Principal level: At least 5 years experience as a senior level safety assessment PTR and internal recognition as an opinion leader in one or more aspects of safety assessment, or the equivalent experience in a similar external organization. Experience of biologics safety assessment required.
2. Advanced knowledge of the many scientific disciplines involved in biopharmaceutical drug safety assessment and the relevant laboratory tools and procedures related to safety assessment and risk management, including PK-PD aspects of study design and data interpretation
3. Documented expertise in scientific and technical problem-solving in an international, multi-disciplinary, project-driven environment.
4. Proficient with full range of techniques used in job and core area?especially with communication and negotiation with global health authorities.
5. Detailed knowledge of drug development processes and worldwide regulatory guidelines and procedures.
6. Ability to manage conflicting expectations in a matrix environment.
7. Proven negotiation skills.
8. Excellent program and project management skills.
9. Team player behavioural attributes.
10. Self-motivated and able to operate independently.
11. Ability to coach and advise colleagues in project-related matters (at senior and principal levels). |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Sr Reagent Dev Associate |
| See above |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Sr Principal Biostatistician |
| Education Minimum/desirable): At least Masters Degree in Statistics (or equivalent degree with 6 years of experience or PhD with 2 years of experience.
Languages: Fluent English (oral or written).
Experience/Professional requirement:
1. Experience in all tasks of a Trial Statistician.
2. Proven knowledge in Statistics and its applications to clinical trials.
3. Proven knowledge of drug development and HA guidelines. Background medical knowledge preferably in relation to the specfic therapeutic area.
4. Proven knowledge of statistical software packages.
5. Good communication and presentation skills. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Sr Principal Biostatistician |
| Education Minimum/desirable): At least Masters Degree in Statistics (or equivalent degree with 6 years of experience or PhD with 2 years of experience.
Languages: Fluent English (oral or written).
Experience/Professional requirement:
1. Experience in all tasks of a Trial Statistician.
2. Proven knowledge in Statistics and its applications to clinical trials.
3. Proven knowledge of drug development and HA guidelines. Background medical knowledge preferably in relation to the specfic therapeutic area.
4. Proven knowledge of statistical software packages.
5. Good communication and presentation skills.
6. Good team player. |
| Millennium Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Sr Mgr, Regulatory Affairs |
|
| Millennium Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Sr Mgr, Clinical Operations (Process Management & Training) |
|
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Sr Med Scient Expert |
| MD or PhD with unique knowledge for successful clinical
program development and execution, with 3-5 years of
clinical research experience required.
- Fluent English (oral and written)
- Advanced medical/scientific writing and communication
skills
? Proven ability to interpret, discuss and represent
efficacy
and safety data relating to the assigned area.
? Proven ability to work both independently or in a cross
functional team setting, including a matrix environment.
? Demonstrated ability to establish strong scientific
partnership with key investigators in assigned TA.
? Medical and/or scientific expertise within a disease area
required; Respiratory expertise preferred |
| Biogen Idec, Inc. |
Cambridge |
MA |
11/20/2009
|
| Sr Manager, R&D Application Support & Training |
ï?§ Proven expertise in the management of scientific software support design, testing, production implementation, and training in a large corporate environment.
ï?§ At least 5 years of software management experience is required, with a minimum of 3-5 years of project management experience.
ï?§ Ability to effectively communicate with customers is essential.
ï?§ Excellent managerial and communication skills combined with proven ability to interact in multi-disciplinary cross-cultural project teams.
ï?§ Experience in a similar position in the biotechnology or pharmaceutical industries is preferred. |
| Johnson & Johnson Family of Companies |
|
CA |
11/19/2009
|
| Sr Engineer - R&D |
| BS degree in relevant discipline and at least five years of related engineering experience is required; or MS degree in relevant discipline and at least three years of related engineering experience. Experience in the medical device industry would be a requirement. Must possess the basic understanding of engineering fundamentals. English communication skills, written and oral is required.Experience with executing design control deliverables is also required. Experience with Cardio Vascular Products will be required in this role.If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Teva Pharmaceuticals USA |
Horsham |
PA |
11/20/2009
|
| Sr Director, Clinical Reg Affairs- Women's Health |
|
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Sr Director Regulatory Affairs |
| Advanced education degree in life-sciences, engineering or public health or law.
1. Greater than 10 years work related profession experience.
2. 7 years experience in drug/diagnostic regulatory affairs.
3. Knowledge of drug development and regulation affairs requirements
4. Familiar with regulatory issues and challenges associated with Drug/Diagnostic co-development and companion diagnostic.
5. Have a track record in successful data submission for FDA and EMEA approval
6. Sound knowledge of international customs and business practice
7. Profound understanding of molecular technologies and the impact on outcomes and diagnostic results
8. Leadership capabilities working across cultures, expertise and backgrounds
9. Excellent negotiation skills with regulatory staff on various levels of hierarchy
10. Outstanding interpersonal and communication skills for bridging scientific and business participants, for negotiating timelines and for effective international collaboration.
11. Outstanding verbal and written communications |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Sr Data Manager |
| Education: Bachelors degree in life sciences, computer science, pharmacy, nursing or equivalent relevant degrees.
Languages: Fluent English (oral and written)
Experience/ Professional Requirements:
1) Ideally 5 or more years experience in drug development with at least 4 years in Data Management activities.
2) Project team leadership experience required.
3) Good technical and problem solving skills.
4) Thorough understanding of clinical trial methodology GCP and medical technology.
5) Ability to work independently, under pressure demonstrating initiative and flexibility.
6) Attention to detail and quality focused.
7) Good organization planning and project management skills.
8) Good interpersonal and communication skills and ability to operate effectively in an international environment.
9) Good negotiation skills.
10) Thorough understanding of physiology, pharmacology, clinical study objectives and the drug development process.
11) Ability to mentor, coach within Data Management and cross functionally and train internal and external partners. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Sr Data Manager |
| Education: Bachelors degree in life sciences, computer science, pharmacy, nursing or equivalent relevant degrees.
Languages: Fluent English (oral and written)
Experience/ Professional Requirements:
1) Ideally 5 or more years experience in drug development with at least 4 years in Data Management activities.
2) Project team leadership experience required.
3) Good technical and problem solving skills.
4) Thorough understanding of clinical trial methodology GCP and medical technology.
5) Ability to work independently, under pressure demonstrating initiative and flexibility.
6) Attention to detail and quality focused.
7) Good organization planning and project management skills.
8) Good interpersonal and communication skills and ability to operate effectively in an international environment.
9) Good negotiation skills.
10) Thorough understanding of physiology, pharmacology, clinical study objectives and the drug development process.
11) Ability to mentor, coach within Data Management and cross functionally and train internal and external partners. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Sr CTH/CTH (nonMD) |
| ? ? 6 years technical, operational and managerial experience in planning, executing, reporting and publishing clinical studies in a pharmaceutical company or contract research organisation.
? Experience in multiple clinical indications and/or TAs is preferable.
? Previous experience leading in parallel several trials; leading multidisciplinary trial teams in a complex matrix environment (including remote).
? Demonstrated ability to establish effective working relationships with key investigators.
? Thorough knowledge of Good Clinical Practice, clinical trial design, statistics, regulatory processes, and global clinical development process.
? Advanced knowledge of the assigned TA is preferred, with the demonstrated capability to interpret, discuss and represent trial or program level data.
? Previous experience in interactions with Health Authorities is preferable.
? Experience in Neuropsychiatric disease areas preferred (i.e. Schizophrenia, bipolar disorder, depression) |
| Biogen Idec, Inc. |
Cambridge |
NC |
11/20/2009
|
| Sr Clinical Logistics Analyst |
- Strong written and oral communication skills
- Ability to multitask on a daily basis and maintain multiple projects in parallel
- Proven capability to work in a fast paced dynamic environment
- Experience in a regulated industry or in an environment dealing with workflow industry contraints (i.e. ISO, ISTA, GMP, etc.)
- Prior Logistics experience
- Cold chain logistics or pharmaceutical logistics experience a plus
Education:
A Bachelor Degree in a technical discipline or Industrial Engineering is required. |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Sr Brand Manager, Hospital & Insitutional |
| See above |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Sr Brand Manager Prevacid Innovation |
| ? Proven track record of securing results on key initiatives within a consumer packaged goods or Rx environment.
? Excellent understanding and demonstrated application of brand strategy.
? Ability to lead an organization toward superior business results.
? Outstanding interpersonal skills, with emphasis on ability to influence others in all functions and at all levels in the organization.
? Understanding of the intricacies of new product development within an OTC environment a must.
? New product development experience a must with NDA experience preferred.
? College degree required, MBA preferred, and 6-8 years CPG Brand experience.
? Well-developed oral, written, and analytical skills.
In addition, this candidate will be involved in all aspects of brand strategy across the portfolio. The successful candidate could have a number of different backgrounds including packaged goods marketing, Rx marketing, market research and brand strategy. The candidate will be an excellent motivator, comfortable with both formal and influential leadership skills. The candidate must be comfortable interacting with and influencing senior management. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Sr Biostatistician |
| At least Masters Degree in Statistics (or equivalent degree) with 5 years of experience or PhD with 2-3 years of experience |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Sr Algorithm Scientist Developer |
| See above |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Sr Admin Asst, Strategic Planning & Operations |
| Minimum 5+ years of solid administrative experience; experience in pharmaceutical and/or healthcare environment preferred
? Excellent interpersonal and written/oral communication skills required
? Some college preferred or related equivalent experience
? The ability to manage multiple assignments with competing priorities in a fast-paced environment is essential
? Must be proactive, efficient, customer-focused and have the ability to work independently
? Must be able to interact effectively with all levels of employees within TS, including international colleagues, and disseminate information in a timely and effective manner.
? Ability to be resourceful, obtain information from the Intranet, and learn new software programs quickly
? Must have proficiency and relevant experience with word processing, spreadsheets, and project management programs. (e.g. MS Office-Word, Excel, PowerPoint, Concur, Lotus Notes, etc.).
? Ability to work in a team environment, attention to detail and strong organizational skills are necessary.
? You must be able to handle confidential information and communicate with all levels of management in both NIBR and Development in a professional manner. |
| Johnson & Johnson Family of Companies |
Albuquerque |
NM |
11/19/2009
|
| Spring Semester Co-op, Ethicon Endo Surgery (ABQ) |
| In order to be eligible for a 2010 Fall R&D Co-op position, candidate must be enrolled in an accredited college/institution and be in good academic standing pursuing a Bachelors or Masters degree in Mechanical Engineering, Biomedical Engineering or related field. Only students in their Sophomore year or above will be considered. A minimum GPA of 3.0 is strongly preferred, with demonstrated leadership/participation in campus programs and/or community service activities. Students must be available to work during session indicated and must be authorized to work in the United States and not require sponsorship in the future. To learn more about Ethicon Endo-Surgery, please visit our website at www.ethiconendo.com. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| SPM/AD, Product Management - Psychiatry |
| This person should have exceptional brand marketing experience and proven success in the areas of brand life-cycle management, professional and medical marketing. Business and/or biological sciences education with concentration on marketing is preferred (MBA a plus). Sales and sales leadership experience are also preferred. Peer influence skills, solid strategic thinking skills, project management and analytical skills are essential.
Strong senior management communication skills and sales force communication skills are essential.
The applicant must possess a high level of analytical and conceptual ability in order to provide strategic focus to the brand, and demonstrate a proven track record of strong execution and results. The ideal candidate will be proficient at uncovering customer based insights and leveraging this knowledge to drive brand strategy and program development. Additional requirements include the ability to lead and manage teams and multiple vendors. 20% travel is required. |
| 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. |
| 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 |
| 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 |
| BD (Becton, Dickinson and Company) |
Research Triangle Park |
NC |
11/20/2009
|
| Software Engineer |
| See above |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Software Developer/ Architect |
| ? Advanced degree in Computer Science from reputable program with top performance.
? Experience building commercial quality web-based software solutions at significant scale with the most advanced tools including both Microsoft-centric and Java-centric platforms.
? Demonstrated ability to work well as part of a high performing software engineering team.
? Interest in intersection between the life sciences and computer science.
? Willingness and ability to use variety of tools in very heterogeneous environment to achieve science and business goals.
? Experience building and managing ?big data? systems- Strong communications and interpersonal skills |
| BD (Becton, Dickinson and Company) |
Holdrege |
NE |
11/20/2009
|
| Six Sigma Coordinator |
| See above |
| International Partnership for Microbicides, Inc. |
|
Paarl |
11/20/2009
|
| Site Development Manager |
| Education/Experience
- Bachelors degree in life science or healthcare field, or equivalent;
- Minimum of five (5) yearsâ?? experience in clinical research;
- Good knowledge of regulatory and ICH/GCP guidelines required;
- Willingness and ability to travel as required (typically requires 50% travel);
- Ability to motivate and mentor, maintain positive interpersonal relationships;
- Familiarity with HIV/AIDS and/or Africa/Asia medical settings is desired;
- End-user computer efficiency, with proficiency in Microsoft Office products.
Knowledge, Skills, and Abilities
- Demonstrated poise and maturity in communicating with high-level executives;
- Excellent time management skills. Demonstrated ability to organize and prioritize multiple projects and tasks;
- Initiative - highly motivated and team oriented, but also able to work independently, assessing priorities and competently handling a variety of activities with a high degree of accuracy in a deadline-driven environment;
- Strong written and verbal communication skills; must be able to communicate effectively;
- Superior attention to detail â?? is thorough when performing work and conscientious about every aspect of work;
- Results orientation - ability to work in a fast-paced environment and meet deadlines with competing priorities.
- Demonstrated proficiency in Microsoft Office products, including Word, PowerPoint and Excel, as well as web-based research and information collection skills required.
This position is based in the Clinical Affairs Department in South Africa IPM office. Job holder should expect fast-paced working environment. |
| International Partnership for Microbicides, Inc. |
|
Paarl |
11/20/2009
|
| Site Development Coordinator |
| Education/Experience
- Bachelors degree in life science or healthcare field, or equivalent;
- Minimum of three (3) years experience in clinical research;
- Good knowledge of regulatory and ICH/GCP guidelines required;
- End-user computer efficiency, with proficiency.
Knowledge, Skills and Abilities
- Demonstrated proficiency in Microsoft Office products, including Word, PowerPoint and Excel, as well as web-based research and information collection skills required;
- Demonstrated poise and maturity in communicating with high-level executives.
- Excellent time management skills. Demonstrated ability to organize and prioritize multiple projects and tasks.
- Initiative-highly motivated and team oriented, but also able to work independently, assessing priorities and completely handling a variety of activities with a high degree of accuracy in a deadline-driven environment.
- Strong written and verbal communication skills; must be able to communicate effectively.
- Superior attention to detail- is thorough when performing work and conscientious about every aspect of work.
- Results orientation- ability to work in a fast-paced environment and meet deadlines priorities.
Terms and ConditionsInternational travel required (60%). Position is based in Paarl, South Africa. |
| 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. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| siRNA Formulations Scientist |
| Ms in gene delivery or related field with 0-3 years of relevant experience in the pharmaceutical industry
Bs in gene delivery or related field with 3+ years of relevant experience in the pharmaceutical industry |
| Agilent Technologies, Inc. US |
Columbia |
MD |
11/20/2009
|
| Signaling Analysis Application Specialist |
| Qualifications:
?Bachelors or Master Degree or University Degree in Electrical/Electronic or Computer Engineering and 5+ years applicable experience in architecting and implementing complex software solutions with a deep understanding of communication protocols (GSM/CDMA/GPRS/UMTS/VoIP/IP).
?Knowledge of Agilent products such as Signaling Analyzer, acceSS7 and or prior experience with telecommunications network monitoring platforms in wire line, cellular telecom, and IP is desired.
?Familiarity with the community?s architecture and interfaces is desired.
?Familiarity with OSI model and current/evolving telecoms standards with a strong background in IP.
?Experience with programming languages C/C++, Perl and Shell Scripting and administration of Operating Systems: Linux and UNIX.
?Strong interpersonal/relationship skills, solid written and verbal communications.
?US citizenship required
?Current US Government Security Clearance -or- ability to process for and obtain US Government Security Clearance is also required.
Position will be located in northern Virginia or Maryland area. |
| 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 |
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 |
| Agilent Technologies, Inc. US |
Houston |
TX |
11/20/2009
|
| Service Sales Specialist ? Southern US Region |
| Requires
- BS/MS in Scientific, Engineering or Business discipline or equivalent.
- 3+ years hands on laboratory or industry experience with instrumentation hardware, software, applications coupled with industry regulatory requirements such as (GLP, GMP, FDA) highly desired
- 3+ years sales experience with a demonstrated track record of success in projects or sales at major accounts highly desired.
- Ability to translate the Value Proposition of service as a financial and operational benefit to meet customer needs.
- Strong business development, sales negotiating, and sales closing skills.
- Must have excellent communication skills (written and verbal) and teamwork skills.
- Outstanding presentation, planning and organizational skills
- High level knowledge of instrument support services business
- Computer literate with advanced skills using Microsoft suite of products (Outlook, Excel, Word, Powerpoint, Access) plus other IT systems.
- Able to interface comfortably at high levels within the customer management structure
- Demonstrated attention to detail and ability to manage large volumes of data.
- Must be available for up to 60% business travel
- Live in Houston, or surrounding communities
Region Includes: Texas, Oklahoma, Louisiana
~cb~11/09/09 |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
11/20/2009
|
| Service Assurance Representative |
| See above |
| Agilent Technologies, Inc. US |
Columbia |
MD |
11/20/2009
|
| Senior System Engineer |
| Qualifications:
?BS/MS in EE or Computer Science and 5+ years of demonstrated experience in architecting and implementing complex solutions for Telco and/or IP Networks.
?Experience in design and/or support using OSI model and current evolutionary trends in Telecoms and IP networks.
?Administration of Operating Systems: Linux and UNIX with working knowledge of Perl and Shell Scripting.
?A broad telecom background and IP technology expertise is essential including UMTS, GPRS, GSM and CDMA technologies and Central Office networking.
?Ability to develop written proposals and participate in the creation of RFI/RFP responses.
?Strong interpersonal/relationship skills with superior verbal and written communication to effectively communicate with the customer, executives and team-members.
?US citizenship required
?Current US Government Security Clearance -or- ability to process for and obtain US Government Security Clearance is also required.Position will be located in northern Virginia or Maryland area. |
| 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 |
| 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. |
| 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
|
| 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. |
| Vertex Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Senior Scientist- Solid State Method Development |
| SKILLS/ABILITIES:
? Solid state chemistry applied to pharmaceuticals
? Experimental design and statistical analysis for Analytical Chemistry
? Computer applications and proficiency
? cGMPs, ICH Guidelines and Compendial Requirements
? Project planning and management
? Oral and written communications
? Mentoring of staff
PERSONAL ATTRIBUTES:
? Motivated self starter
? Team player
? Ability to lead small scientific group
? Committed to quality
? Well organized, efficient worker
? Good interpersonal skills
? Good problem solver
? Creative, innovative thinker
? Developer of people
? Easily adaptable to change
? Brings closure to work in a timely manner
EDUCATION AND EXPERIENCE:
PhD in Chemistry or materials science in related field with 7+ years of experience, Masters Degree in Chemistry with 10+ years of experience, or Bachelors Degree in Chemistry with 12+ years of experience or equivalent.
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain. Vertex co-discovered the HIV protease inhibitor, Lexiva, with GlaxoSmithKline.
Vertex Pharmaceuticals |
| Vertex Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Senior Scientist, Process Safety |
| - Ph.D. or BS/MS in Chemical Engineering or Chemistry
- 6 + years of relevant work experience in API or fine chemical process development, scale-up, troubleshooting, and optimization
- A strong and sound understanding of synthetic organic chemistry and chemical engineering fundamentals along with common chemical hazards/incompatibilities with a familiarity with modern in-situ process analysis tools (FTIR, n-IR, UV-Vis) being a plus
- Experience with the application of common safety evaluation instrumentation such as TGA, DSC, RC-1, ARC, RSST and the resulting data in the identification and mitigation of chemical process hazards
- Demonstrated experience with modeling complex, physicochemical systems and statistical design of experiments as well as a fluency with common physical property and process modeling tools (Aspen, Dynochem, Matlab, etc.)
- Knowledge of applied kinetics, thermodynamics, and transport fundamentals
- A nature driven by high productivity and producing results
- The ablity to generate and implement original ideas and solutions that contribute materially to the success and development of drug substance candidates
- Excellent communication and interpersonal skills, strong organization and planning skills, a high level of technical aptitude and creativity, and the ability to interact, lead, and collaborate within an interdisciplinary team environment comprised of organic, physical, and analytical chemists; project team members; and manufacturing personnel
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company?s strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex?s product pipeline is focused on viral diseases, inflammation, autoimmune diseases, cancer, pain and bacterial infection.
Vertex Pharmaceuticals |
| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| Senior Scientist - Neuroscience Biology |
| ·PhD plus minimum 2 years of post-doctoral research experience, demonstrated ability to implement independent research as evidenced by a strong publication record related to the desired core discipline.
Preferred Background:
·Behavioral Neuroscience or comparable discipline.
|
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Senior Scientist (Pharmacokinetics) |
| M.S. degree in biological or related sciences with minimal 3 years laboratory experience. Research experience using animal models is mandatory. Small animal surgical experience is highly desired. Excellent verbal and written communication skills are essential. The knowledge of radiochemistry, tissue distribution, metabolism and pharmacokinetics is desirable. Prior work experience with PK/PD analysis and a demonstrated ability to work with modeling tools and databases (e.g. WinNonlin, GastroPlus, Watson, Spotfire, etc) is a plus.
THIS REQUISITION APPROVED BY TSLT ON 1-JULY-2009 AND MOVED TO CRITICAL HIRE LIST. |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
11/20/2009
|
| Senior Scientist |
| See above |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Senior Scientific Expert: Development Licensing & Evaluation |
| University degree (diploma, PhD or MD)
1. 8 years experience within pharmaceutical industry
2. 3 years of Project management or cross functional experience
3. Advanced level of the basic science. Bring an expert level of understanding in a functional area
4. Thought Leader for the drug dev. process; expert at aligning development program goals with business needs
5. Advance knowledge of business, competitive environment and of international business practices
6. Advanced planning and tracking skills, able to see big picture, well-organized, focused on results
7. Expert leadership skills demonstrated in GPT, in staff management role or in other organizational assignments. Expert skill to optimize contribution of team members as individuals and members of a cohesive team.
8. Strong interpersonal and communication skills for bridging between scientific and business participants, for negotiating timelines and for effective international collaboration. Strong verbal communication. Expert in written communications. Strong, critical and objective interpretation of scientific and commercial information. Expert team player |
| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| Senior Safety Medical Director - Renal |
| Requirements ?Education and Experience
Given the breadth of roles encompassed by this opportunity, it is recognized that some requirements may be more relevant to certain specific positions and, therefore, the following criteria are intended as guidance:
· Specialty training and board certified/eligible in nephrology
· MD background with strong expertise in nephrology, ideally drug-induced kidney injury.
· > 5 years of drug development/safety experience the majority of which should be in industry with clear evidence of delivery
· UK physicians will be expected to have completed Higher Medical Training in Pharmaceutical Medicine
· Recognized by peers for therapeutic area expertise and commercial/safety understanding
· Experience in supervising physicians
· Ability to balance business and clinical research objectives
· Experience working with regulatory agencies, preparing regulatory documents and overseeing submissions.
· A thorough knowledge of the pharmaceutical industry, especially clinical research and global regulatory requirements and practices governing expedited and periodic safety reporting, signal generation, safety evaluation and risk management activities
· Proven high quality scientific record.
· Demonstrated capability to lead implementation of new technology and/or working routines within a complex organization.
· Excellent verbal and written communication skills.
· Experience in leading of cross-functional teams.
· Broad knowledge of drug development.
Skills and Capabilities
· Strong team-working skills and an ability to work collaboratively in a global pharmaceutical environment
· Strategic thinking
· Strategic influencing
Organizational Behaviors
· Foster behaviors that reinforce AZ as a global organization
· Ensure respect for different practices and expertise in different environments
· Ensure inclusivity of appropriate medical and scientific expertise in strategic and tactical decision-making
Reporting Relationship
· If applicable, this section contains a list of positions that report to the position, either directly or indirectly
· Reports ? none
|
| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| Senior Safety Medical Director - Hepatic |
| Requirements ?Education and Experience
Given the breadth of roles encompassed by this opportunity, it is recognized that some requirements may be more relevant to certain specific positions and, therefore, the following criteria are intended as guidance:
· Specialty training and board certified/eligible in hepatology
· MD background with strong expertise in hepatology, ideally drug-induced liver injury.
· > 5 years of drug development/safety experience the majority of which should be in industry with clear evidence of delivery
· UK physicians will be expected to have completed Higher Medical Training in Pharmaceutical Medicine
· Recognized by peers for therapeutic area expertise and commercial/safety understanding
· Experience in supervising physicians
· Ability to balance business and clinical research objectives
· Experience working with regulatory agencies, preparing regulatory documents and overseeing submissions.
· A thorough knowledge of the pharmaceutical industry, especially clinical research and global regulatory requirements and practices governing expedited and periodic safety reporting, signal generation, safety evaluation and risk management activities
· Proven high quality scientific record.
· Demonstrated capability to lead implementation of new technology and/or working routines within a complex organization.
· Excellent verbal and written communication skills.
· Experience in leading of cross-functional teams.
· Broad knowledge of drug development.
Skills and Capabilities
· Strong team-working skills and an ability to work collaboratively in a global pharmaceutical environment
· Strategic thinking
· Strategic influencing
Organizational Behaviors
· Foster behaviors that reinforce AZ as a global organization
· Ensure respect for different practices and expertise in different environments
· Ensure inclusivity of appropriate medical and scientific expertise in strategic and tactical decision-making
Reporting Relationship
· If applicable, this section contains a list of positions that report to the position, either directly or indirectly
· Reports ? none
|
| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| Senior Safety Medical Director - Cardiac |
| Requirements ?Education and Experience
Given the breadth of roles encompassed by this opportunity, it is recognized that some requirements may be more relevant to certain specific positions and, therefore, the following criteria are intended as guidance:
· Specialty training and board certified/eligible in cardiology/cardiovascular disease
· MD background with strong expertise in cardiology, ideally drug-induced cardiac injury.
· > 5 years of drug development/safety experience the majority of which should be in industry with clear evidence of delivery
· UK physicians will be expected to have completed Higher Medical Training in Pharmaceutical Medicine
· Recognized by peers for therapeutic area expertise and commercial/safety understanding
· Experience in supervising physicians
· Ability to balance business and clinical research objectives
· Experience working with regulatory agencies, preparing regulatory documents and overseeing submissions.
· A thorough knowledge of the pharmaceutical industry, especially clinical research and global regulatory requirements and practices governing expedited and periodic safety reporting, signal generation, safety evaluation and risk management activities
· Proven high quality scientific record
· Demonstrated capability to lead implementation of new technology and/or working routines within a complex organization.
· Excellent verbal and written communication skills.
· Experience in leading of cross-functional teams.
· Broad knowledge of drug development.
Skills and Capabilities
· Strong team-working skills and an ability to work collaboratively in a global pharmaceutical environment
· Strategic thinking
· Strategic influencing
Organizational Behaviors
· Foster behaviors that reinforce AZ as a global organization
· Ensure respect for different practices and expertise in different environments
· Ensure inclusivity of appropriate medical and scientific expertise in strategic and tactical decision-making
Reporting Relationship
· If applicable, this section contains a list of positions that report to the position, either directly or indirectly
· Reports ? none
|
| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| Senior Safety Medical Director - Cardiac |
| Requirements ?Education and Experience
Given the breadth of roles encompassed by this opportunity, it is recognized that some requirements may be more relevant to certain specific positions and, therefore, the following criteria are intended as guidance:
· Specialty training and board certified/eligible in cardiology/cardiovascular disease
· MD background with strong expertise in cardiology, ideally drug-induced cardiac injury.
· > 5 years of drug development/safety experience the majority of which should be in industry with clear evidence of delivery
· UK physicians will be expected to have completed Higher Medical Training in Pharmaceutical Medicine
· Recognized by peers for therapeutic area expertise and commercial/safety understanding
· Experience in supervising physicians
· Ability to balance business and clinical research objectives
· Experience working with regulatory agencies, preparing regulatory documents and overseeing submissions.
· A thorough knowledge of the pharmaceutical industry, especially clinical research and global regulatory requirements and practices governing expedited and periodic safety reporting, signal generation, safety evaluation and risk management activities
· Proven high quality scientific record
· Demonstrated capability to lead implementation of new technology and/or working routines within a complex organization.
· Excellent verbal and written communication skills.
· Experience in leading of cross-functional teams.
· Broad knowledge of drug development.
Skills and Capabilities
· Strong team-working skills and an ability to work collaboratively in a global pharmaceutical environment
· Strategic thinking
· Strategic influencing
Organizational Behaviors
· Foster behaviors that reinforce AZ as a global organization
· Ensure respect for different practices and expertise in different environments
· Ensure inclusivity of appropriate medical and scientific expertise in strategic and tactical decision-making
Reporting Relationship
· If applicable, this section contains a list of positions that report to the position, either directly or indirectly
· Reports ? none
|
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Senior Roles-Regulatory Affairs, R&D |
| 10+ years extensive Regulatory Affairs experience. An academic background in biological/medical sciences (preferably MD or PhD), strong diplomatic skills for dealing with regulatory agencies ability to realize a vision by inspiring and motivating others, ability to thrive and grow in a fast-paced, intellectually challenging environment, are additional important requirements. Candidate should be fluent in English. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Senior Roles-Global Product Development R&D |
| M.S. in Pharmaceutics or related science; PhD preferred
Experience: ? 10 -15 years experience in similar fast-paced regulated industry, OTC industry preferred.
? Diverse and extensive understanding of new drug delivery technologies in Pharmaceutical and related fields
? Proven track record of developing and launching new and innovative products in aggressive timeframes
? Excellent leadership, communication and presentation skills
? Entrepreneurial spirit, strong sense of urgency & drive, results-oriented
? Ability to realize a vision by inspiring others,
? Strong core competency in leading diverse pharmaceutical disciplines in a Team environment toward productive outcomes.
? Able to interact effectively with the most senior levels of management both internally and externally |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Senior Roles-Global Drug Safety & Pharmacovigilance -R&D |
| Education : MD required
Experience: ? Minimum 10 years experience in health care or pharmaceutical industry
? Minimum 4 years of experience in Drug Safety
? Minimum 4 years management experience |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Senior Roles-Clinical Development & Medical Affairs, R&D |
| ? MD degree
? 10+ years experience in the Pharmaceutical industry in OTC and/or Rx Clinical research with commercial savvy
? Experience with development of overall clinical strategy and development plans
? Proven management experience at a senior level
? Demonstrates leadership behaviours by providing vision and direction
? Proven knowledge of drug development processes
? Be able to effectively liaise and influence internally and externally
? Excellent communication and interpersonal skills
? Fluency in written and spoken English, knowledge of French or other European languages beneficial but not essential |
| Johnson & Johnson Family of Companies |
Jacksonville |
FL |
11/19/2009
|
| SENIOR RESEARCH OPTOMETRIST |
| A minimum of a Bachelors Degree in Optometry, Doctoral Degree in Optometry, PhD in Vision Sciences or MD with specialty in Ophthalmology is required. Post-graduate degree or residency in cornea and contact lenses preferred. A minimum of one year working experience in clinical research of contact lens products or vision science is preferred. It is required for the candidate to have patient care experience. General knowledge, understanding and application of principles, concepts and practices of clinical research are preferred. Working efficiently under pressure, ability to manage multiple projects simultaneously is required. Strong organizational, communication and analytical skills is required. Familiarity with Optics and Wavefront aberrations are preferred. MS/PhD in Physiological Optics is preferred. |
| Johnson & Johnson Family of Companies |
Jacksonville |
FL |
11/19/2009
|
| SENIOR RESEARCH OPTOMETRIST |
| A minimum of an OD degree is required. A MS degree or Formal Corneal and Contact Lens residency program is preferred. A minimum of 2 years experience in clinical research of contact lens products is preferred. Very good oral and written communication skills are required. Knowledge, understanding and application of principles, concepts and practices of clinical research are preferred. Strong organizational, communication and analytical skills are preferred. The ability to manage multiple projects simultaneously is required. Experience with studies under IRB (Investigative Review Board) / Ethics Committee / or FDA (Food and Drug administration) review is preferred. Proficiency in Word, Excel, PowerPoint 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! |
| 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. |
| 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. |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
11/20/2009
|
| Senior Regulatory Affairs Specialist |
| See above |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Senior R&D roles- Category Leads |
| 10-15 years of Pharmaceutical industry experience and/or Over the Counter experience in NRT
? Extensive working knowledge in development along with experience in one or more R&D functional areas (clinical, regulatory)
? Demonstrated track record of leading a complex (e.g. cross-functional, matrix designed) project team
? Demonstrated use of communication and change management strategies/tactics to influence new ways of thinking and working
? Track record of selecting, coaching and developing talent in the organization
? Successfully working across boundaries and building strong external relationships
? Success in situations requiring rigorous, analytical problem solving and the ability to determine scientific opportunity and commercial targets
? Success in effectively communicating and influencing decisions with senior management
? Understanding of global regulatory requirements and impact of public relations
? Mastery of team leadership necessary to work collaboratively with diverse parts of the business, such as marketing
? Demonstrated understanding of the interdependencies of scientific results and commercial possibilities and the use of this knowledge to make appropriate business decisions
? Awareness of cultural differences in different geographic areas and in potentially different approaches to development by an external partner
Education : Phd, Life Sciences or Medical Degree (MD) preferred |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Senior Quality Engineer, Pen Injection Platform |
| See above |
| 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 |
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! |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Senior Project Engineer - Molding |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Senior Project Engineer - Assembly |
| See above |
| 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 |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Senior Product Manager - Vaccines |
| See above |
| Johnson & Johnson Family of Companies |
Irving |
TX |
11/19/2009
|
| Senior Polymer Engineer |
| A minimum of a Master's or advanced degree in a scientific, engineering, or related discipline is required, with a PhD preferred. A minimum of 5+ years of experience in polymer chemistry or a related discipline is required. Knowledge of product design in relation to Medical Device Directives, ISO13485 and 21CFR820 regulations and standards is required, with knowledge of QSR, Canadian Medical Device Regulations, and Japanese Medical Device Regulations an asset. Hands-on experimentalist background with experience in polymer characterization and silicone chemistry is an asset. Understanding of material characterization, structure-property, and utilization towards intended application is an asset. Experience in medical device product development is required. Experience in medical device process development and regulatory process is an asset. Knowledge of Design/Process Excellence (Six Sigma, Lean, etc.) is an asset. Knowledge of Biostatistics, FEA, and Solidworks is an asset. A demonstrated ability to work independently and in team-oriented environments, embracing change, risk, and flexibility will be needed. Must be capable of handling multiple projects/tasks at the same time as well as the ability to listen to customers' needs and develop solutions to meet their requirements. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Senior Pathologist |
| DVM/MD degree (or equivalent) with graduate training in pathology plus 10 years experience in toxicologic pathology, or PhD in veterinary pathology plus 5 years experience in toxicologic pathology. Ability to interpret toxicologic pathology results and write reports and scientific manuscripts. Ability to supervise other personnel, when necessary. Board certification in related fields is preferred (e.g., ACVP, DABT). |
| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| Senior Patent Litigation Attorney |
| · JDdegree plus 6-8 years employment in patent litigation as a private practice litigation attorney or in-house litigation counsel.
· Litigation-team management experience.
· Excellent oral and written communications skills, and human relations skills.
Preferred:
· Patent litigation experience in Hatch-Waxman matters or cases involving pharmaceutical or biotechnology arts.
· An educational background in biology, biochemistry, chemistry or similar arts
· Registration in the US Patent and Trademark Office.
|
| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| Senior Patent Attorney (Multiple Positions) |
| · BS/MS ? Organic Chemistry and JD
·7+ years of patent experience
· Background in organic/medicinal chemistry
· Significant experience preparing and prosecuting small molecule patent applications
· Excellent interpersonal skills
· Strong communication skills
Preferred Background
· PhD in Organic Chemistry
· Global patent experience in the pharmaceutical industry
|
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Senior Paralegal - Procurement Contracts |
| See above |
| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| Senior Medical Information Manager |
| ? Advanced degree in Pharmacy (PharmD preferred), Pharmacology, Science or equivalent clinical experience
? Pharmacy Licensure preferred
? 2+ years experience in pharmaceutical industry based Drug Information Delivery or equivalent industry experience
? Demonstrated expertise in drug information communication and management
? Excellent oral and written communication skills and interpersonal skills
? Knowledge of FDA requirements
? Ability to apply Regulatory and Compliance guidelines to Drug Information delivery
? Understanding of the information needs for various customer segments
? Project Management leadership experience
? Strong leadership ability
Preferred Background
? Clinical Pharmacy experience with patient care exposure
? Drug Information Residency or equivalent experience
Skills and Competencies
? Expert Scientific Knowledge
? Leadership Skills
? Drug Information Management Expertise
? Regulatory and Compliance Expertise
? Organization Savvy
? Communication Skills
? Presentation, Facilitation and Instructional Skills
|
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
11/20/2009
|
| Senior Marketing Manager, Strategic Marketing |
| See above |
| BD (Becton, Dickinson and Company) |
Durham |
NC |
11/20/2009
|
| Senior Marketing Manager ? Multiplexed Assay Products |
| See above |
| 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 |
| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| Senior Manager; Brand Corporate Affairs |
| ? BS/BA degree in Communications, Marketing or a related field
? 5 - 7 years Communications experience
? Effective communicator: written, verbal and presenting to groups
? Experience managing PR agencies and managing $MM+ budgets
? Brand technical knowledge
? Knowledge of the pharmaceutical industry
? Working knowledge and experience with marketing objectives and business strategies
? Demonstrated understanding of and ability to perform effectively and successfully in the industry and in the environment in which it operates.
Skills and Competencies:
? Strong writing skills-both internal and external audiences
? Media relations skills and training
? Project management skills
? Strategic planning and influencing skills
? Strong interpersonal skills and able to build strategic working relationships
? Listens attentively and responds constructively to the needs, viewpoints, and interests of others.
? Effective communicator: verbal and written.
? Demonstrates strategic thinking, planning and strategic influencing capabilities.
? Communicates an aligned, clear vision for the future role of his/her own work unit with clearly focused priorities
? Takes initiative, makes decisions, operates independently and is an effective team member, operates interdependently, builds consensus decisions
? Demonstrates general business literacy, knowledge and acumen along with demonstrated proficiency in functional/technical/professional discipline.
? Comfortable and competent problem-solver; solution-oriented; not constrained by process or precedent
? Demonstrates ability to be influential by identifying key stakeholders, adapting approach to gain their commitment and delivering business objectives
Preferred Background:
? Experience with issues management desirable
? Background in public affairs or journalism is preferred
? Healthcare PR or agency experience is preferred
|
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Senior Manager, Nucleic Acid Technology Chemistry & Testing |
| At least five years of In Vitro Molecular Diagnostic Product/Sample Prep/Assay development experience with a successful track record of regulatory submission and/or product launch. Minimum of five years of supervisory and managerial experience including budgeting, project planning, resource allocation, and staff development. Demonstrated technical proficiency and ability to collaborate with others across functional disciplines. Experience in Design for Six Sigma (DFSS) is highly desirable. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Senior Manager, Nucleic Acid Technology Chemistry & Testing |
| At least five years of In Vitro Molecular Diagnostic Product/Sample Prep/Assay development experience with a successful track record of regulatory submission and/or product launch. Minimum of five years of supervisory and managerial experience including budgeting, project planning, resource allocation, and staff development. Demonstrated technical proficiency and ability to collaborate with others across functional disciplines. Experience in Design for Six Sigma (DFSS) is highly desirable. |
| 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 |
| Millennium Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Senior Manager, Internal Communications |
|
| Johnson & Johnson Family of Companies |
Memphis |
TN |
11/19/2009
|
| Senior Logistics Analyst (1 of 2) |
| A minimum of a Bachelor's degree required, preferably in Logistics, Business, Operations, Engineering or related field. MBA preferred. A minimum of 4 years experience in Global Logistics, Supply Chain, Manufacturing or Distribution is required. Experience working in a Good Manufacturing Practices (GMP) environment is preferred. Previous experience in Medical Devices and Diagnostics is preferred. Experience or training in Process Excellence (Lean/Six-Sigma) is required. Process Excellence/Six Sigma certification preferred. Must have excellent verbal and written communication skills. Must have strong organizational and analytical skills. Knowledge of Warehouse Management Systems (i.e. MARC, SAP) preferred. Knowledge of Microsoft Office (Word, Excel, PowerPoint, Outlook) is required. Project management experience preferred. Change leadership experience preferred. Experience collaborating with all levels of management in a cross-functional team environment is required. 5% travel is required. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| Vertex Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Senior Linux Engineer |
| ? Perform day-to-day administrative support for Linux (CentOS, Redhat) environments
? Install,Configure & Deploy Linux servers.
? Experience with monitoring tools (ex: Groundworks, BigBrother)
? Experience with data protection software (eg CommVault)
? Experience supporting Oracle 10g Production Databases
? 5+ years experience in a 300+ server environment
? 5+ years of Linux systems administration
? RedHat Linux 3.x through 5.x
? Strong Scripting (Perl, Shell, etc) abilities
? Excellent communication skills both written and verbal
? Strong organization and problem solving skills, as well as willingness to work cross-functionally with other teams in the organization.
? VMWare experience a plus
? Citrix experience a plus
? Research, Pharmaceutical & FDA regulated experience a plus
This position will help to support our San Diego office. Because of this, we are looking for someone able to work a 9 am-6 pm or 10 am -7 pm EST shift.
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain. Vertex co-discovered the HIV protease inhibitor, Lexiva, with GlaxoSmithKline.
Vertex Pharmaceuticals |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Senior Intellectual Property Counsel |
| See above |
| Vertex Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Senior Financial Systems Analyst |
| Minimum Requirements:
Bachelor?s degree in Computer Science, Engineering, Finance or Accounting and 4+ years of relevant work experience. Leadership attributes and demonstrated ability to work with more senior staff. Demonstrated strong analytical skills; ability to understand, trouble shoot, process map, and efficiently explain complex financial systems. Prior working knowledge of a major ERP (Oracle) and financial planning tool (SAP/Outlooksoft, Cognos, Hyperion) a must. Independent worker with demonstrated ability and willingness to take on new projects and work with teams.
Familiarity or experience with pharmaceutical research and development process a plus, but not required. Flexibility to work in a fast paced and dynamic work environment.
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain. Vertex co-discovered the HIV protease inhibitor, Lexiva, with GlaxoSmithKline.
Vertex Pharmaceuticals |
| Johnson & Johnson Family of Companies |
New Brunswick |
NJ |
11/19/2009
|
| Senior Financial Analyst - multiple positions (NJ & PA locations) |
| A minimum of a bachelors degree is required preferably a major in Accounting or Finance. A MBA is preferred. A CPA, CMA, or other financial certifications are preferred. A minimum of three years finance or related business experience is required. Experience in the pharmaceutical, medical device, or consumer products industries as well as public accounting is preferred. Candidate must possess excellent analytical (MS Excel), conceptual, communication and interpersonal skills. The ability to think creatively and work in a team environment is required. Individual must work well in a dynamic environment and be able to recommend and implement process improvements, work independently and handle multiple tasks simultaneously. The ability to effectively take on leadership roles in various functions is required. |
| Vertex Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Senior Financial Analyst |
| Minimum Requirements
-Bachelors? degree and 3+ years of experience in Financial Analysis
-Strong leadership and communication skills. This position requires frequent interactions with various levels throughout the organization.
-Solid presentation skills. Ability to present financial and nonfinancial data together effectively.
-Flexibility to adjust to changing pace and needs of the organization.
-Ability to work independently and exercise judgment.
-Ability to develop and improve financial and business processes.
-Ability to work in collaborative environment
-Proven financial leadership
Desired skills/background
-Accounting experience
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain. Vertex co-discovered the HIV protease inhibitor, Lexiva, with GlaxoSmithKline.
Vertex Pharmaceuticals |
| Novartis Oncology |
na |
FL |
11/20/2009
|
| Senior Finance roles |
| Education :CPA, MBA
Languages: Fluent English; additional languages are a plus
Experience: - At least 10 years of broad-based financial experience acquired in companies with rigorous and very efficient financial systems
- Experience in headquarters functions and operational finance experience from working in a region or national affiliate
- Experienced in financial responsibility for large scale units
- Several years of management experience, ideally a team of more than 10 |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Senior Finance roles |
| At least 10 years of broad-based financial experience acquired in companies with rigorous and very efficient financial systems |
| 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. |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Senior Engineer, Quality Systems |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Senior Engineer, Packaging Technology, BD Medical Surgical Systems |
| See above |
| 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 |
Cambridge |
MA |
11/19/2009
|
| Senior Engineer |
| Minimum of a Bachelor's Degree or equivalent in Computer Science, Information Systems, Engineering, or related technical discipline (required)
8+ years of experience in security engineering
Integration of AD and LDAP directory stores for authentication (AD) and directory attributes for administration roles, event management, and reporting
Windows, linux, unix, networking technologies experience
Lotus Notes experience a plus
Certifications a plus
Must possess good communication and mentoring skills
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain. Vertex co-discovered the HIV protease inhibitor, Lexiva, with GlaxoSmithKline.
Vertex Pharmaceuticals |
| 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
|
| 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
|
| 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! |
| Astellas Pharma, Inc. |
Deerfield |
IL |
11/19/2009
|
| Senior Director, Quality Assurance |
| 1. Minimum BA / BS or equivalent, advanced degree preferred, with 15 years of industry experience, 10 years of QA experience, and minimum of 6 years managing staff.2. Comprehensive knowledge of GxP and other regulations for pharmaceuticals and biologics and understanding of global quality standards and regulatory authority inspection trends relating to product development, submission and commercialization. Demonstrated knowledge and experience with quality oversight of global clinical trials and pharmacovigilance operations. Demonstrated ability to establish local and regional Quality policies and to influence the development and implementation of global Quality policies in support of the quality system.3. Effective written and oral communication and interpersonal skills, facilitation, negotiation and influencing skills with an demonstrated ability to drive, champion and negotiate organizational support for strategic initiatives, projects or programs, both internally and externally within Astellas group and with external stakeholders. Plays a key role in the identification and implementation of long-term business planning strategies, assuring quality is taken into consideration.4. Demonstrated ability to provide leadership for key strategic issues and significant QA policies, practices and processes with respect to quality compliance with minimal executive management oversight. 5. Demonstrated experience in making decisions to resolve the most complex problems and in providing sound compliance advice and direction in a manner that has a significant impact across the Astellas Group and external stakeholders.6. Demonstrated ability to anticipate, proactively respond to trends, and/or shifts in the external environment (e.g., regulatory, business partner relationships, industry standards) and to predict impact to quality assurance and/or Astellas business.7. Track record of effective management and development of quality assurance professionals. Demonstrated ability to both lead and manage the Quality Assurance department, comprised of multiple functional quality assurance units. |
| Astellas Pharma, Inc. |
Deerfield |
IL |
11/19/2009
|
| Senior Director, IT Account Management and Shared Services |
| ? Advanced Degree or equivalent experience required.? Ten plus years related experience required. Pharma industry preferred.? Extensive knowledge and skill through broad and/or deep experiences in IT. ? Strong communication and interpersonal skills, capable of motivating and influencing teams.? Perform at the highest levels and able to make decisions independently.? Able to translate between technical and business leaders at the highest levels.? Viewed as credible, and well respected by the business and IT organizations.? Accountability in building and maintaining positive and cooperative working relationships. ? Collaboration and cross functional facilitation skills.? Demonstrated understanding of project management, quality assurance, and IT best practices.? Proficiency with commercial applications that are designed to support enterprise wide business capabilities. |
| Astellas Pharma, Inc. |
Deerfield |
IL |
11/19/2009
|
| Senior Director Marketing - Urology |
| REQUIREMENTS:- BA/BS degree with advance degree preferred plus 10-12+ years of relevant experience (depending on degree) required.- Senior directors have an in-depth understanding of multiple, related fields. Ability to set strategy for a department and related company functions. Requires significant communication and leadership skills and the ability to create and implement the department?s mission and integrate it with that of the company?s. - Recognizes problem situations and uses both formal and informal methods to find solutions. Makes independent decisions on the most complex problems. Develops policies that avoid recurrence.- Has responsibility for a major segment of the company. Decisions significantly impact the company?s financial or public relations positioning. Serves as a principal spokesperson for a department or division. - Manages a department consisting of direct reports at the manager and director level.- Establishes and prioritizes area?s project portfolio. Projects usually managed through subordinates and often span across departments and are of major significance. |
| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| Senior Director Field Medical Physician (CV) |
| · Graduate of a recognized medical school and recipient of an M.D. degree
· Range of 11 - 33 years of clinical practice
· Board certification in cardiology
· Background in academic medicine, clinical research, and familiarity with biostatistics
· Excellent written and oral communication, interpersonal, and organization skills
· Demonstrated ability to proactively and positively engage teams through multiple communications channels including telephone, e-mail, Internet, and face-to-face
· Ability to travel nationally and internationally
Preferred Background
· Other training such as an M.P.H. or other advanced degree
· Experience with or business acumen around working within the pharmaceutical industry
· Experience with pharmaceutical drug development and medical/scientific affairs
· National recognition as a key opinion leader as demonstrated by a track record of scholarship, independent research funding, publications, and membership in national societies
· Familiarity with DDMAC, PhRMA code, and key regulations in the pharmaceutical industry
· Geographically located close to Wilmington, Delaware headquarters
|
| 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. |
| 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 |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Senior CQA Compliance Specialist |
| BA/BS or equivalent.
English (optimally a second universal language preferred).
5+ years clinical/industry/health authority experience with at least 2 years GCP auditing experience.
30-40% travel.
Ability to manage and objectively evaluate compliance issues.
Ability to maintain a moderate degree of independence with respect to decision making and problem solving.
Excellent verbal and written communication skills, team player, interpersonal skills.
Excellent computer skills, including Excel, Word, etc.
Thorough knowledge of the clinical development, clinical research processes and drug registration process/requirements required.
Thorough knowledge of GCP regulations and guidelines as well as in applicable Novartis SOPs/NIPs and Business Practices.
Good knowledge of computer validation and Part 11 requirements.
Previous experience identifying training needs, developing and conducting training programs.
Ability to multi-task and function independently as required.
Ability to operate successfully in various team capacities, including leader and/or active member.
Ability to operate successfully in various cultural environments.
Ability to coach and mentor.
Auditor certification a plus. |
| Johnson & Johnson Family of Companies |
Irwindale |
CA |
11/19/2009
|
| Senior Complaints Analyst |
| A minimum of a Bachelor's degree in an Engineering, Life Sciences, Scientific, Nursing, or related discipline is required. A minimum of 5+ years experience in a highly regulated industry is required, with experience in an FDA (Food & Drug Administration) regulated environment required. Experience in an ISO (International Organization for Standardization) environment preferred. Knowledge of GP (Good Practices) requirements from manual to electronic processes and HIPPA (Healthcare Information Patient Privacy Act) is preferred. Proficiency with Microsoft Office, specifically with Microsoft Excel is required. Experience with Statistical Software packages (Minitab or other) is preferred. Complaint management/input system experience such as Seibel, Oracle, or a similar system is a plus. Knowledge of Medical Device, MDR (Medical Device Reporting), MDV (Medical Device Vigilance), and/or worldwide reporting is preferred. Experience working on CAPAs is an asset. Familiarity with tracking and trending processes is considered an asset. Outstanding written and verbal skills, as well as great interpersonal skills are required. An individual with strong Leadership Skills, experience with Project Management, and who is investigative and analytical is strongly preferred. This position will require 10% travel and will be based in Irwindale, CA. 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) |
Durham |
NC |
11/20/2009
|
| Senior Clinical Trial Manager |
| See above |
| BD (Becton, Dickinson and Company) |
Durham |
NC |
11/20/2009
|
| Senior Clinical Research Associate (IVD strongly preferred) |
| See above |
| 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. |
| Morphotek®, Inc. |
Exton |
PA |
11/19/2009
|
| Senior Clinical Quality Assurance Specialist |
| Job Requirements and Qualifications
BA/BS degree in biological sciences, nursing or related discipline, or equivalent experience required
Strong knowledge of government regulations, guidelines and standards for investigation of new pharmaceutical products is required
Experience in QA audits of Clinical Investigators
Experience in QA audits of Clinical documents associated with clinical trials
Experience in system/process audits
Experience in development of SOPs
Working knowledge and understanding of drug development and global clinical regulatory environment
Ability to manage multiple projects
Effective organizational skills
Effective team player and detail oriented
Strong attention to detail, good organizational skills, ability to work independently
Solid oral and written communication skills with ability to communicate effectively and professionally with medical personnel
Knowledge Requirements:
Knowledge of the code of federal regulations, European Directives, ICH/GCP practices. The candidate will also have a working knowledge of clinical auditing processes. Previous participation in regulatory inspections is a plus.
Experience:
A minimum of 3-5 years working experience as a clinical quality assurance auditor.
Other Information
Special Information (Travel required, physical requirements, on-call schedules, and etc.):
Travel 25-35%
|
| 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
|
| 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
|
| 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. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Senior Chemist |
| This position requires candidate to be currently enrolled in a PhD program in Chemistry or Biochemistry. Ideal candidate will possess superior communication and interpersonal skills. Must be graduating between August 2009 and August 2010. Candidates must be eligible to work in the US without sponsorship. Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. To be considered for this position, please visit our career site at www.merck.com/careers. At this site you can search our "University Opportunities", create a profile and submit your resume for requisition # CHE002034. |
| Merck & Co., Inc. |
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. |
| Novartis Oncology |
na |
CO |
11/20/2009
|
| Senior Buyer/Planner |
| Educational/Professional Requirements:
BS/BA with 3-5 years purchasing experience
Knowledge equivalent to and/or receipt of ISM or APICS certification
Skills & Competencies:
? Working knowledge of MRP/MPS methodology and understands inputs and outputs of a material requirements planning system (MRP).
? Demonstrated knowledge and ability to use common software tools such as spreadsheets and word processors.
? Effective planning and organizational skills to ensure all tasks are completed within prescribed timelines.
? Effective written and oral communication skills.
? Problem solving skills to address supply issues within this position?s means of delegated authority.
Physical Demands:
This position requires close and distance vision, occasional lifting up to 25 pounds, and being seated a majority of the time.
Work Environment:
Typical office enviornment with moderate noise levels. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Senior Biostatistician |
| Provide statistical consultation and analysis in support of research & development, clinical testing, and manufacturing of Novartis MDx products.
The incumbent will:
-Have Ph.D. or Master?s with 5+ years in Statistics or Biostatistics
-Support internal clients through out MDx.
-Represent Biostatistics on project teams and serve as primary liaison to key internal clients with regard to resource needs and timelines.
-Interact with FDA or other regulatory agencies as needed in statistical aspects of study design, data analysis and statistical procedures; interpret the project implications of regulatory guidelines.
-Manage, mentor direct reports, and provide them opportunities for their self development
-Develop Biostatistics procedures and guidelines to comply with corporate quality polices
-Provide technical leadership and initiate methodological research to improve the methods current in use. |
| 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
|
| AstraZeneca Pharmaceuticals |
Boston |
MA |
11/19/2009
|
| Senior Associate Scientist ? Compound Management |
| Minimum years experience:
?Typically 3 or more years experience in a Biotech / Pharmaceutical setting post Bachelor's Degree or equivalent
Competencies (knowledge and skills):
?Well-developed understanding of theoretical aspects of discipline and a high level of ability in experimental techniques.
?Regularly demonstrates capacity to apply literature and theoretical concepts to the advancement of project goals.
?Strong knowledge and understanding of relevant database and analytical software.
?Independent planning, execution and interpretation of experiments that contribute significantly to project goals.
?Able to develop logical positions and convince others.
?Highly productive: consistently generates high quality results within established time frames.
?Strong problem solving skills and the ability to, on the basis of their own experience and analytical skills, initiate the use of new techniques and to ascertain their value in solving problems relating to their immediate project.
?Collects, analyzes, and summarizes data for reports and patents, and presents data at project and/or team meetings.
?Delivers presentations that are well thought out, informative and convincing. Able to present work at internal meetings and external meetings when appropriate.
?Communicates effectively with colleagues at all levels, showing well-developed verbal and written communication skills, coupled with an ability to listen, resulting in clear and succinct messages and accurate interpretation of feedback.
?Communicates relevant information from meetings or literature to colleagues.
?Identifies and rapidly informs supervisor and colleagues of issues critical to attainment of project goals and is realistic in ability to overcome problems.
?The ability to manage multiple tasks efficiently.
Behaviors:
?Is reliable, has strong work ethic, and respect for colleagues.
?Commitment to team goals.
?Willingly shares expertise and ideas and is viewed as a resource by colleagues.
?Is candid and honest in discussions.
?Demonstrates flexibility, open-mindedness, and adaptability.
?Act in accordance with all AstraZeneca policies on personnel, SHE, best laboratory practice, etc.
?Expands personal skills and knowledge as required to be effective.
?Projects creditability and professionalism
?Fosters environment of scientific excellence, innovation, productivity and timeliness by example.
Leadership Capabilities:
Passion for Customers: Understands one?s customers and uses that insight to provide value
Thinks Strategically: Quickly identifies and acts on opportunities, combining forethought with action. This is based on an understanding of the external environment and its impact on AZ.
Acts Decisively: Makes and acts on decisions quickly and effectively and fosters the same in others. This is based on an underlying courage to enable risk taking for the business.
Drives Performance: Holds self and others accountable for the achievement of performance expectations. Creates an environment that enables others to perform at their best.
Works Collaboratively: Actively creates and promotes cross boundary collaboration with the aim of archive better business results. Boundaries can exist between individuals, geographies, cultures, teams, functions or organisations.
Develops People and Organisation: Demonstrates and genuine commitment to the time and effort needed to develop oneself and others.
|
| 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 |
| Teva Pharmaceuticals USA |
Fairfield |
NJ |
11/20/2009
|
| Security Officer |
|
| Johnson & Johnson Family of Companies |
Seattle |
WA |
11/19/2009
|
| Seattle, WA: Alternate Care Representative: Ethicon Products, Unit of Ethicon Inc. |
| To be considered for this role, candidates must meet the following criteria: A minimum of a Bachelor's degree, at least three years of outside selling experience, excellent written and oral communication skills, a valid driver's license and clean driving record, the ability to travel as necessary (potentially overnight and/or weekend) is preferred required. The ability to work in a lab or an operating room environment is also required. It is preferred that candidates have documented successful sales performance (high growth, results vs. plan). Be a self-starter with strong time management and planning skills, have the ability to target accounts and achieve results through a daily action plan, and be able to collaborate with other J&J associates (peers, marketing, Strategic Account Managers), external companies (distributors) and KOL's. Suture Sales experience and Distribution Sales is highly preferred but not required. If you want to explore the many small-company environments behind the big company impact of the Johnson & Johnson Family of companies, bid on this position today. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| SDC Compliance Associate - Quality R&D |
| BS/MS in a science field with 8-10 years experience in the pharmaceutical industry.
o Good knowledge and understanding of all GMP related requirements, proficiency of regulatory and ICH guidelines
o Broad experience in the pharmaceutical industry with a strong analytical and/or manufacturing background, some R&D a plus.
o Detail oriented with Quality Assurance background with good problem solving acumen.
o Ability to work effectively in a team environment with great organization skills
o Excellent communication skills
o Critical thinking, process and performance oriented. Constant drive to improve working practices
o Provision of timely and accurate documentation to minimize submission deficiencies
o Proven performance in review of key documents by highlighting areas of deficiencies and aiding in remediation of the documentation.
o Timely follow-up and closure of Deviations, Investigations, Change Controls and CAPAs.
o Initiation of trainings and/or other appropriate measures to enhance quality and compliance within department
o Escalation of issues/alerts as appropriate to Upper Management and proposal of corrective actions |
| 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! |
| 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. |
| Vertex Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Scientist/ Senior Scientist |
| The competitive candidate will have an MS or PhD in Pharmaceutics, Chemistry, Chemical/Biochemical Engineering, or Biophysics (or equivalent) with a strong mathematical modeling background.
-The ability to work in a highly cross functional team environment is essential, including the ability to communicate at a technical level with members of research, pharmaceutical development, drug metabolism and clinical pharmacology groups. The candidate should have demonstrated the ability to develop complex mathematical models to simulate and analyze compound behavior in clinical and non-clinical systems.
-Previous experience in PK modeling using Gastroplus, WinNonlin and NONMEM is a plus. Several years of industrial experience in Pharmaceutical Development would further distinguish the candidate.
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain. Vertex co-discovered the HIV protease inhibitor, Lexiva, with GlaxoSmithKline.
Vertex Pharmaceuticals |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Scientist-Biochemical & Organ Toxicology |
| Technical Skill Sets
? Good skills in isolating and cultivating cells from different organs in different species
? Good skills in performing a variety of biochemical techniques (e.g., preparation of cell and tissue extracts, subcellular fractionation, enzyme assays, ELISA, Western blots, ?).
? Good skills in performing a variety of molecular biology techniques (e.g. nucleic acid purification, cloning, PCR)
? Good understanding of SOPs as well as their practical implementation
? Fluency in English
? Working knowledge of relevant IT systems
Experience
? At least 3 years of experience in cellular biology or toxicology in either academic or industrial environment
? Working experience with mammalian cell culture models (primary cultures and cell lines) and related techniques
? Working experience in molecular & biochemical analytical techniques
Personal Skill Sets:
? Interpersonal and teamwork skills
? Good oral communication and writing skills
? Computer skills for experimental organization, assay design, data collection and analysis, and report writing
Education
Bachelor or Master degree in life sciences, preferably biochemistry, pharmacology or biology. |
| 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. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Scientist, Pharmacokinetics |
| EDUCATION/EXPERIENCE:
Ph.D. with 1-3 years or MS with 5-8 years of experience in one or more areas biopharmaceutics, pharmacokinetics, drug metabolism, bioanalytical chemistry, biostatistics, PK modeling, in vivo-in vitro correlation (IVIVC), and clinical endpoint BE study design/conduct. Inhalation experience a plus. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Scientist, NPKPD |
| M.S. degree in biological or related sciences. Research experience using animal models is mandatory. Small animal surgical experience is highly desired. Good verbal and written communication skills are essential. The knowledge of radiochemistry, tissue distribution, metabolism and pharmacology is desirable. Prior work experience with PK/PD or statistical analysis and a demonstrated ability to work with modeling tools and databases (e.g. WinNonlin, GastroPlus, Watson, Spotfire, etc) is a plus. |
| 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. |
| Morphotek®, Inc. |
Exton |
PA |
11/20/2009
|
| Scientist, Bioanalytical Development |
| Knowledge/Skills/Abilities Required
• BS/MS with 5-7 yrs or PhD with 0-2 yrs relevant experience required.
• In-depth knowledge and understanding of bioanalytical assays for protein macromolecules with strong scientific and technical skills in method development and validation.
• A minimum of 5 years of hands-on experience in the development and/or validation of quantitative ligand binding and immunogenicity assays for biologics (e.g. antibodies, proteins or peptides).
• Well versed in current regulatory guidance and industry practices for development and validation of bioanalytical methods for large molecule biologics.
• Excellent verbal and written communication skills.
• Experience in GLP and/or clinical regulatory compliance is desired.
• Strong analytical skills, and a demonstrated ability to work both independently and in a team setting required.
|
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Scientist or Scientific Associate, Formulations |
| A Ph.D. in Pharmaceutical Sciences, Biochemistry, Chemical Engineering or related life science field with a 0-2 years of post-doctoral experience or an M.S. in relevant field with 2-3 years of Biotechnology/Pharmaceutical industry experience is preferred.
In-depth knowledge of protein structure, chemistry and various degradation and aggregation mechanisms and should be able to apply these principles for designing stable formulations.
Hands-on expertise in liquid and lyophilized formulation development is highly desirable.
Hands-on experience with various biophysical and physio-chemicall characterization techniques, such as CD, FTIR, fluorescence, DSC, light scattering, size-exclusion chromatography, gel electrophoresis etc is highly desired.
Candidate should be detail-oriented and demonstrate problem solving and organization skills.
You must be a strong team player and have the ability to multi-task. |
| Novartis Oncology |
na |
NC |
11/20/2009
|
| Scientist IV, Process Dev-TO |
| Education/Experience:
Minimum BS degree in scientific, engineering or life sciences area. 5-8- years with BS; 3-6 years with MS; 0-3 year with PhD or JD |
| 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
|
| Biogen Idec, Inc. |
Cambridge |
MA |
11/20/2009
|
| Scientist II, Stability |
Minimum of 3 years direct experience in stability / formulation of biological and/or small molecule products in the Pharmaceutical industry, with 10+ years industry experience.
PhD with 10+ years industry experience preferred, or BS/MS degree in Biology, Chemistry, Biochemistry, Chemical/Biochemical Engineering, or related disciplines with equivalent experience. |
| 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. |
| Biogen Idec, Inc. |
Cambridge |
MA |
11/20/2009
|
| Scientist II, BioPharm Develop |
â?¢Experience in solid state chemistry and material science technology.
â?¢Expertise in pre-formulation (characterization of physiochemical properties).
â?¢Experience in drug discovery support and solubilizing techniques to support medicinal chemistry, pharmacology, DMPK and PCDS.
â?¢Expertise in polymorphism, salt screening/salt selection |
| Biogen Idec, Inc. |
Cambridge |
MA |
11/20/2009
|
| Scientist II, Bioanalytical |
| A Ph.D. in cell biology/molecular biology/immunology with 5-7 years of industry experience in a related field is required. Experience in immunoassay development, cell based assay development using a variety of technologies such as ELISA, Biacore, flow cytometry, reporter gene assays, statistical analysis of data is required. Familiarity with PK/PD concepts, and experience in supporting pre-clinical and clinical studies, interaction with pharmacokinetics scientists, toxicologists, clinicians and with regulatory authorities is desirable. Familiarity with GLP compliance procedures and guidelines is a must. |
| Vertex Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Scientist II, Analytical Development |
| - A Ph.D., Master's, or Bachelor's degree in the life sciences or physical sciences with a preference for a concentration in Chemistry, Analytical Chemistry or Pharmaceutical Chemistry
- 3+ years (PhD), 5+ years (MS) or 8+ years (BS) current, relative industry experience working in drug substance and drug product support
- A broad understanding of the drug development process, including clinical design, chemical development, and formulation development, especially how these processes impact analytical method development, validation, and method transfer
- Working knowledge of the risks that exist in all aspects of method development, validation and transfer and the ability to use risk analysis and quality-by-design (QbD) approaches to develop robust methods, design appropriate validation protocols to validate methods for their intended use, and ensure successful method transfer are essential
- Experience working with in ICH and FDA method validation guidelines with preference for the ability to identify areas overlooked by these guidelines
- Hands-on GMP experience with a preference for a background in developing GMP friendly methods
- Skilled in HPLC, LC-MS, GC, GC-MS, FT-IR, UV-VIS, KF, NMR, dissolution and other instruments
- The ability to work successfully in team/matrix environment as well as independently
- The ability to work in a fast pace environment, to manage priorities, and to maintain timelines for multiple projects
- Excellent written and verbal communication skills
Although Vertex does not have an active opening, we are interested in establishing relationships with well qualified and talented individuals for future opportunities in our Analytical Development group in Cambridge, MA.
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company?s strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex?s product pipeline is focused on viral diseases, inflammation, autoimmune diseases, cancer, pain and bacterial infection.
Vertex Pharmaceuticals |
| BD (Becton, Dickinson and Company) |
San Diego |
CA |
11/20/2009
|
| Scientist II - Molecular Biology |
| See above |
| 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. |
| Millennium Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Scientist I/Scientist II, Molecular Technologies |
|
| 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. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Scientist I, Mammalian Cell Line Development |
| A B.S. or M.S. degree in biology, cell biology, immunology, or related life science field and 3 plus years of experience in biotechnology or pharmaceutical industry are required.
Recent Ph.D. graduates will also be considered.
The Scientist must be able to work independently to design experiments and perform therapeutic protein expression and production runs to accomplish team goals. Candidate should bring a highly collaborative spirit with an ability to work on multiple projects and maintain well organized records and notebooks.
The successful candidate should also have excellent written and oral communication skills, and be able to thrive in our fast-paced and dynamic organization. |
| Vertex Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Scientist I, Chemical Engineer |
| - A Ph.D. degree with 1+ years of pharmaceutical industry experience; an MS degree with 3+ years of pharmaceutical industry experience; or a BS degree with 6+ years of pharmaceutical industry experience. Degrees with a life science concentration required, with a preference for concentrations in chemical engineering or chemistry.
- A demonstrated understanding and working knowledge of chemistry and chemical engineering fundamentals; advanced technical knowledge and experience in API process development, process scale-up, troubleshooting, and optimization; applied kinetics, thermodynamics, and transport fundamentals; as well as familiarity with modern laboratory instrumentation (HPLC, GC, FTIR, Raman, FBRM, DSC, TGA, XRPD, etc), automation tools, and laboratory/plant implementation of PAT
- Experience with modeling complex, physicochemical systems; data analysis; statistical design of experiments; QbD concepts, and fluency with common physical property and process modeling tools (Aspen, Dynochem, Matlab, etc.)
- A track record of successful laboratory and pilot-scale development in the areas of reaction engineering, catalysis, crystallization, separation technologies, drying, and micronization
- The ability to successfully interact, lead, and collaborate within an interdisciplinary team environment comprised of organic, physical, and analytical chemists; project team members; and manufacturing personnel
- Experience with the management of external scientific activities and CRO/CMO relationships
- Proven communication (verbal and written) and interpersonal skills
Vertex Pharmaceuticals |
| Biogen Idec, Inc. |
Cambridge |
MA |
11/20/2009
|
| Scientist I, BioPharm Development |
â?¢Experience and expertise in HPLC, Dissolution, GC/MS (headspace for residual solvents), solid state characterization: PSD, XRPD, TGA, DSC, BET, VTI etc. This includes method development (quantitative and qualitative).
â?¢DHA: is able to write protocols and reports to conduct the compatibility testing supporting the IND and other regulatory filings.
Education: PhD in Analytical Chemistry
BS: 6+yrs, MS: 4+yrs and PhD: 2+yrs |
| 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 |
| 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 Jose |
CA |
11/20/2009
|
| Scientist I |
| See above |
| Agilent Technologies, Inc. US |
Garden Grove |
CA |
11/20/2009
|
| Scientist I |
| MS/Ph.D. or equivalent industrial experience required
Strong protein chemistry background essential:
- conjugation
- purification
Experience working with immunoglobulins desired
Diagnostics industry experience desired
~cb~11/11/09 |
| AstraZeneca Pharmaceuticals |
Delaware |
DE |
11/19/2009
|
| Scientist Bio Science |
| Minimum Requirements
?PhD plus minimum 2 years of post-doctoral research experience, demonstrated ability to implement independent research as evidenced by a strong publication record related to the desired core discipline.
Preferred Background
?Behavioral Neuroscience or comparable discipline.
Reporting Relationship
?Direct Reports ? none initially
?Indirect Reports - supervise a team of up to two colleagues
Leadership Capabilities
Passion for Customers: Understands one?s customers and uses that insight to provide value
Thinks Strategically: Quickly identifies and acts on opportunities, combining forethought with action. This is based on an understanding of the external environment and its impact on AZ.
Acts Decisively: Makes and acts on decisions quickly and effectively and fosters the same in others. This is based on an underlying courage to enable risk taking for the business.
Drives Performance: Holds self and others accountable for the achievement of performance expectations. Creates an environment that enables others to perform at their best.
Works Collaboratively: Actively creates and promotes cross boundary collaboration with the aim of archive better business results. Boundaries can exist between individuals, geographies, cultures, teams, functions or organisations.
Develops People and Organisation: Demonstrates and genuine commitment to the time and effort needed to develop oneself and others.
|
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Scientist - Animal Models Laboratory |
| The preferred candidate will therefore have strong experience in animal experimentation design and execution, drug administration, and small animal surgery. The preferred candidate will have knowledge of mechanisms of drug pharmacology and toxicity and biological approaches to study such mechanisms.
Specific responsibilities include execution of diverse animal experiments. The candidate will help the AM Lab Head plan, interpret and present experimental results. The candidate is expected to work autonomously, requiring minimal guidance on major activities, and to collaborate productively and cooperatively with Laboratory Animal Support (LAS) services. Secondary responsibilities include laboratory maintenance, ordering, oversight of junior technical staff, regular participation to project team meetings as assigned, maintaining orderly and up-to-date laboratory records in accordance with best practices for a GLS-practicing (GLP-like) laboratory.
BA, BS, MS required in life sciences or relevant related field. Medical, surgical, veterinary, or specialized animal experimental training is preferred.
Experience
- In vivo pharmacology.
- Small animal surgery.
- Coordination and cooperation with existing animal study support services and personnel.
- Laboratory Management.
- Molecular & cellular biology skills/techniques.
Technical Ability
- Drug administration to animals, including PO, IV, IP.
- Small animal surgery, such as adoptive cell transfer, vascular dissection, etc.
- Collection of body fluids from living small animals, such as urine and blood.
- Small animal necropsy and tissue collection.
- Molecular and biochemical techniques, such as PCR-based genotyping, qPCR, Western blotting, ELISA, and multiplex immunoassays
- Laboratory maintenance.
- Cost and inventory control at the laboratory level.
- Excellence in data summarization.
Presentation
- Excellent oral and written communication skills. Able to independently summarize role of team, experimental approaches and findings, and potential value.
- Able to present and defend data in lab meetings, as well as during external liasing and project team meetings.
- Able to prepare written reports, for AM, Translational Toxicology, iTox, and external consumption.
Three-five years minimal required years of experience
Rational/Justification: Senior Scientist Technical position essential to support work in the laboratory. Translational Safety Biomarkers and Animal Models (TSBAM) is a new laboratory with a mission to provide innovative, fit-for-purpose animal models for project-driven safety studies. We have hired only the Lab Head of the Animal Models Lab, and lack technical support for delivery of defined objectives. This technical position is prioritized to support the Lab activities aligned with the overall safety strategy, and to move high priority activities forward. |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
11/20/2009
|
| Scientist |
| See above |
| Southern Research Institute |
Frederick |
MD |
11/20/2009
|
| Scientific Project Leader for Emerging Pathogens |
| Seeking qualified candidate with a PhD in life sciences discipline, MD, or DVM with a minimum of eight years prior experience managing NIH grants, contracts or projects in the biotech or pharmaceutical industry environment. Must be proficient in project management methodologies, have demonstrated success in generating/developing funding streams through successful proposal submissions; an outstanding publication record and documented combination of education, experience, and training to qualify as a study director within specified programs. Must be able to lead execution of large complex projects involving multiple technical staff at varying levels of expertise. Must be able to respond quickly to new funding opportunities while, at the same time, provide support to existing projects. Prior successful experience in a Contract Research Organization is highly preferred. Qualified candidate must be able to positively interact and communicate with individuals across the organization at all levels and positively engage current and potential funding sponsors within the government and private sector. Candidate must be able to work in a team environment and be capable of supporting and participating in related ongoing project lead by others. Must be able to be able to collaborate with others to accomplish a common goal.
Prior documented experience working in infectious disease research, particularly virology, immunology, biomarkers, and animal models (small animal or NHP models) of infectious diseases. Well known standing in the field of human pathogenic viruses preferred. Experience in respiratory viruses, antiviral therapeutics, or vaccine discovery and development preferred. Prior GLP experience preferred. Must be able to obtain clearance for select agents. This position will work in a BSL2 and BSL3 plus environment and therefore must be able to meet the medical and vaccination requirements.
This position is responsible for obtaining funding for and ensuring the successful execution of projects awarded. This position, as the study director of awarded projects, is responsible for the overall technical conduct of the study; interpretation, analysis, documentation, and reporting of results; issuance of study protocols and amendments; adherence to study protocols and amendments; following GLP practices; meeting all contract deliverables; and maintaining a positive relationship with the client. This position also ensures the quality of the product or service delivered; manages project budget and risk factors; and uses project management methodologies to ensure that projects are managed effectively. We operate in a matrix environment. This position may or may not have direct reports. Regardless of direct reporting technical staff, this position is responsible for the supervision of any/all individuals supporting the project to ensure high quality outcomes. This position is responsible for providing performance feedback to individuals supporting projects through informal and formal performance management processes. This position coordinates necessary technical talent with other project leaders and supervisors to ensure project needs are met. This position trains and develops others as necessary, provides mentoring and coaching, and seeks input from others when necessary. Prior supervision/leadership experience helpful. This position will report to the Director of Infectious Disease Research or the Program Leader.
Work Environment & Conditions: Individuals who will enter BSL-2/BSL-3 labs must: satisfactorily complete medical requirements; obtain applicable vaccinations; pass and maintain in depth security and background checks, including clearance to handle select agents; wear required PPE; and must have effective communication skills. All offers of employment (and continued employment) are subject to drug testing.
Applications must be made online at http://www.southernresearch.org / for position sr-02194
|
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Scientific Education Manager, Chemistry |
| PhD in chemistry with 3-5 years of experience in pharma/biotech as a medicinal chemist. Experience in scientific education, web-based learning tools, DMPK, or pharmacology is a plus. Domestic and international travel will be required. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Scientific Education Manager ? Translational Sciences |
| MD, or PhD with strong research experience in life sciences, clinical sciences, or pharmacology, and at least 3 years of postdoctoral training or professional experience in the biopharmaceutical industry. The candidate must have a working knowledge of early drug development. Experience with clinical trials and/or in initiating scientific education programs or training is a plus. Domestic and international travel will be required. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Scientific Associate II, Protein Design |
| This role requires a BS or MS in Biology, Biochemistry, Molecular Biology or Immunology and a minimum of 3 years of relevant
working experience. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Scientific Associate II, Protein Design |
| This role requires a BS or MS in Biology, Biochemistry, Molecular Biology or Immunology and a minimum of 3 years of relevant
working experience. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Scientific Associate II, Protein Design |
| This role requires a BS or MS in Biology, Biochemistry, Molecular Biology or Immunology and a minimum of 3 years of relevant
working experience. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Scientific Associate BS/MS In Vivo Pharmacology Ophthalmology |
| BS or MS degree in biology, physiology, pharmacology, immunology, cellular biology, or related discipline; minimum of 1 year experience, preferably in the pharmaceutical or biopharmaceutical industry; broad scientific foundation, strong work ethic, excellent oral and written communication, and ability to function in an interdisciplinary team setting are essential. |
| BD (Becton, Dickinson and Company) |
Durham |
NC |
11/20/2009
|
| Scientific Affairs Liaison |
| See above |
| 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 |
| Johnson & Johnson Family of Companies |
|
NJ |
11/19/2009
|
| SAP Senior Financial Analyst (Skillman, NJ) |
| A minimum of a bachelors degree is required; a concentration in information technology, accounting and / or finance is strongly preferred. A minimum of 5 years of finance/accounting experience is required. A minimum of 5 years of SAP FICO functional experience is required. A MBA/MA/MS in business administration, MIS, accounting or finance is strongly preferred. Experience in the pharmaceutical, medical device or consumer products industries is preferred. Able to identify and diagnose SAP issues/opportunities and develop solution options is required. Able to generate complete and accurate financial postings is required. Candidate must possess excellent analytical (MS Excel), conceptual, communication and interpersonal skills. The ability to think creatively and work in a team environment is required. Individual must work well in a dynamic environment and be able to recommend and implement process improvements, work independently and handle multiple tasks simultaneously. The ability to effectively take on leadership roles in various functions is required. Individual must be able and willing to travel 10 - 15% of the time and be prepared to support financial closing cycles as required. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| SAP NetWeaver Java Application Architect |
| - University degree or equivalent in Information Technology experience
- more than 6 years of IT experience out of which last 4 years in the development and design of SAP NetWeaver Java applications (SAP Enterprise Portal and Composition Environment)
- Experience in design and governance of SAP NetWeaver Java development processes and standards desired
- Active participation in at least 2 complete implementation project cycles from blue print till post go-live support as a SAP NetWeaver Java developer
- In-depth knowledge and working experience with Enterprise Portal, Composition Environment and NetWeaver Development
- Sound knowledge of the SAP NetWeaver technology platform and related products (SOA, ESR and others)
- Java background
- Knowledge of ABAP programming language advantageous
- Excellent communication skills with a strong customer focus
- Excellent analytical skills, solution and target oriented |
| 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 |
|
CA |
11/19/2009
|
| Santa Barbara, CA: Inside Sales Representative: Mentor Corporation |
| To be considered for this role, candidates must meet the following criteria: Bachelor's degree from a four-year college or university, and one to two years related experience preferred. Inside sales experience within the aesthetics or medical device industry strongly preferred. Knowledge of clinical, surgical techniques and procedures, and medical terminology. Skills in demonstrating a professional phone manner. Must work independently and plan extensively to meet goals. Ability to maintain accuracy, consistency and quality in a fast-paced, multitask environment. 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
|
| 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 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 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 |
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! |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Sales Representative/Consultant - Red Bank, NJ - 1ZEK1C |
| A Bachelor's Degree * Outside sales experience with documented success in business-to-business sales preferred. * Professional accomplishments that reflect self-motivation, initiative, independence, and strong customer service orientation. In return, you'll be rewarded with: * An outstanding benefits package that includes a 401(K) and vision plan * An excellent salary and incentive awards program * A company automobile and paid expenses * Ongoing quality classroom and field training * Professional career development/growth opportunities and an educational assistance program.
Novartis is an equal opportunity employer M/F/D/V. |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Sales Representative/Consultant - Morristown, NJ - 1ZEB4B |
| A Bachelor's Degree * Outside sales experience with documented success in business-to-business sales preferred. * Professional accomplishments that reflect self-motivation, initiative, independence, and strong customer service orientation. In return, you'll be rewarded with: * An outstanding benefits package that includes a 401(K) and vision plan * An excellent salary and incentive awards program * A company automobile and paid expenses * Ongoing quality classroom and field training * Professional career development/growth opportunities and an educational assistance program.
Novartis is an equal opportunity employer M/F/D/V. |
| Novartis Oncology |
na |
OH |
11/20/2009
|
| Sales Representative - Toledo South, OH - 3ZAE4B |
| A Bachelor's Degree * Outside sales experience with documented success in business-to-business sales preferred. * Professional accomplishments that reflect self-motivation, initiative, independence, and strong customer service orientation. In return, you'll be rewarded with: * An outstanding benefits package that includes a 401(K) and vision plan * An excellent salary and incentive awards program * A company automobile and paid expenses * Ongoing quality classroom and field training * Professional career development/growth opportunities and an educational assistance program. Novartis is an equal |
| 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%+
|
| 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.
|
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Sales Consultant/Sr. Sales Consultant - New Brunswick, NJ - 1ZEK4A |
| A Bachelor's Degree * Outside sales experience with documented success in Long Term Care and or Account Management experience. Alzheimer selling experience preferred. * Professional accomplishments that reflect self-motivation, initiative, independence, and strong customer service orientation. In return, you'll be rewarded with: * An outstanding benefits package that includes a 401(K) and vision plan * An excellent salary and incentive awards program * A company automobile and paid expenses * Ongoing quality classroom and field training * Professional career development/growth opportunities and an educational assistance program.
Novartis is an equal opportunity employer M/F/D/V. |
| Astellas Pharma, Inc. |
Deerfield |
IL |
11/19/2009
|
| Sales Analyst |
| REQUIREMENTS:- Bachelor Degree in a relevant field.- 2-4 years of analytical experience that includes data analysis and reporting.- Pharmaceutical Industry experience preferred.- Possess strong interpersonal skills with the ability to effectively interact with all levels of employees including senior management.- Proficient in Microsoft Excel, Access, PowerPoint and/or SAS.- Working knowledge of one or more programming techniques such as SAS, Microsoft Access, Excel, VBA macro is a plus.- Must possess working knowledge of various statistical modeling techniques and their application within complex analytical projects, e.g., regression modeling, promotion response modeling, ROI, correlation coefficient, etc.- Must possess excellent verbal and written communication skills, attention to details, and the ability to multitask.- Excellent organizational, planning and project management skills with a strong attention to detail and ability to effectively manage cross-functional projects.- Ability to work independently in a dynamic fast paced environment, with minimal supervision.- Demonstrated ability in taking initiative to proactively evaluate existing sales strategies and recommend changes, when appropriate.- Working knowledge of sales data sources, i.e., IMS Health, Wolters Kluwer Health and SDI is preferred. |
| Merck & Co., Inc. |
Elkton |
VA |
11/19/2009
|
| Safety and Industrial Hygiene Manager |
| Requirements: Bachelor's degree required. Concentrations in Safety, or Industrial Hygiene strongly preferred. Relevant professional certifications and/or Six Sigma Green belt a plus. Minimum of 10 years applied safety professional work experience in a pharmaceutical, chemical or manufacturing environment, coupled with 3 years in a position of safety program leadership. Excellent leadership, program management, project management, and organizational skills. Demonstrated experience in developing facilities to meet OSHA VPP certification criteria or equivalent. Broad based knowledge of safety regulations. Customer focus-team building, proactive style. Excellent verbal and written communication skills. Proven record interpersonal and negotiation skills. Provenience in MS Word, MS Excel, MS Powerpoint. Consistently cited as a great place to work, we discover, develop, manufacture and market a wide range of vaccines and medicines to address unmet medical needs. Each of our employees is joined by an extraordinary sense of purpose - bringing Merck's finest achievements to people around the world. We offer an excellent salary and an industry-ranked benefits program, including tuition reimbursement, work-life balance initiatives and developmental programs at all levels. Merck's retirement package includes a pension plan and one of the best 401(k) plans in the nation. To be considered for this position, please visit our career site at www.merck.com/careers to create a profile and submit your resume for requisition # ENV000115.Merck is an equal opportunity employer, M/F/D/V - proudly embracing diversity in all of its manifestations. Our work is someone's hope. Join us.Where patients come first - Merck Search Firm RepresentativesPlease Read Carefully: Merck is not accepting unsolicited assistance from search firms for this employment opportunity. Please, no phone calls or emails. All resumes submitted by search firms to any employee at Merck via-email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck. No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means. |
| 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! |
| Agilent Technologies, Inc. US |
El Segundo |
CA |
11/20/2009
|
| RF and Microwave Field Applications Engineer |
| Position requires Bachelors or Master Degree or equivalent and a minimum of 1-2yrs relevant experience with typically 2-4yrs in an Applications Engineering or Sales support role.
? Candidate must be knowledgeable of competition and able to identify lockout specification (identify Agilent's competitive advantage over competition)
? Must be able to analyze customer requirements and recommend appropriate solutions
? Must possess excellent communication skills
? Must be US Citizen
~cb~11/13/09 |
| Merck & Co., Inc. |
Montreal (West Island) |
QC |
11/19/2009
|
| Researcher in Process Chemistry (Ph.D.), temporary mandate 12 months |
| Education and experience: We are looking for a chemist with an Ph. D. degree in synthetic organic chemistry with a demonstrated skill set (publications, presentations) and who is a creative analytical thinker and has a keen interest to apply his/her talents to the discovery process for new drug molecules. The chosen candidate must be prepared to join a multidisciplinary team and be involved in the entire drug discovery process. Organic synthetic experience in the field of anti-infectious agents will be considered an asset. Ideally the candidate will have completed post doctoral studies and have a minimum of 2 years industrial experience.Language requirements: Good English communication skills (oral and written) are required. Bilingualism, English & French would be an asset. |
| Merck & Co., Inc. |
Montreal (West Island) |
QC |
11/19/2009
|
| Researcher in Chemistry (BS.c/MS.c level), Temporary position 12 months |
| Education and experience: We are looking for a chemist with an B.Sc /M. Sc. degree in synthetic organic chemistry with a demonstrated skill set (publications, presentations) and who is a creative analytical thinker and has a keen interest to apply his/her talents to discover new drug molecules. The chosen candidate must be prepared to join a multidisciplinary team and be involved in the entire drug discovery process. Personal research efforts are also encouraged and applicants should demonstrate interest to contribute to their field. Organic synthetic experience in the field of anti-infectious agents will be considered an asset. Language requirements: Good English communication skills (oral and written) are required. Bilingualism, English & French would be an asset. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Research Scientist-Pre-clinical MRI |
| A BS/MS or PhD degree in Bioengineering, or related field.
A minimum of one year experience with small animal Magnetic Resonance Imaging is required. PET experience is a plus. |
| 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 |
| Vertex Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Research Scientist I/II |
| The ideal candidate for this position will have at least an MS degree with 6 years, or a PhD with 4 years of hands-on experience in using relevant general pharmacology assays, such as Langendorff perfusion, telemetry, plethysmography, gastric emptying and intestinal transit, or renal function test. Demonstrated ability to analyze, interpret, and report physiological function data is a must. Industry experience and experience with assessing drug-induced QT prolongation is preferred. Extensive knowledge of Data Sciences/Ponemah (P3P and DataQuest) or similar software packages is necessary. Ability to write basic programs using SAS software for data analysis and statistics is a plus. Good team work, strong written and oral communication skills are required, including good report writing and presentation skills.
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 |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Research HSE Risk Manager |
| This position requires 3-5 years experience in health, safety, and environmental risk assessment and management in a biotech/ pharma laboratory environment. The successful candidate should have experience in implementation and maintenance of HSE audit systems, development of tools and programs, and will have conducted periodic audits and follow up for corrective measures.
Bachelor degree in life sciences, chemistry, or other appropriate discipline and ABSA certification as a Certified Biosafety Professional (CBP) or other equivalent certification in Occupational Health and Safety Program is required. Solid verbal and written English communication skills. Fluency in additional languages, such as German or Mandarin would be favorably considered. Demonstrated leadership abilities, as well as the ability to communicate and influence others in a complex, matrixed environment are essential. |
| 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
|
| 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. |
| 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
|
| 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
|
| 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, 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, 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, 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, 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. |
| BD (Becton, Dickinson and Company) |
San Diego |
CA |
11/20/2009
|
| Research Associate III |
| See above |
| 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 |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Research Associate ? X-ray crystallography |
| B.S/M.S. or equivalent in biochemistry or a related discipline with at least 2 years of research laboratory experience. Experience in protein chemistry (e.g. expression, purification and characterization) is required. Experience with protein crystallization, x-ray data collection, and/or biophysical characterization of proteins would be a decided asset. The candidate must possess good oral and written communication skills. |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Research Associate ? Muscle |
| BS/MS degree in biology or equivalent with 3 to 5 years of bench experience in either academic or industrial research setting.
In vivo work: experience in various injection techniques, tissue collection and processing is required. Histology and Immunohistochemistry: sectioning, staining and image analysis/interpretation is a plus.
Biochemistry: protein purification, immunoprecipitation, gel electrophoresis and Western blotting.
Molecular Biology: PCR/RT-PCR, primer design and optimization is a plus.
Cell culture: sterile techniques, cell passaging, cryo-preservation and recovery.
Effective communication skills, attention to detail, ability to work effectively on project teams, self-starter attitude, and intellectual curiosity |
| 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 |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Research Associate - In Vivo Physiology ? Muscle Disease |
| The role requires:
BS/MS degree in physiology, pharmacology, animal science or related fields with 3-5 years experience in a pharmaceutical industry or academic setting
Strong in vivo skills are essential
Experience with models of muscle disease/dysfunction and muscle electrophysiology preferred
Good interpersonal and communication (both oral and written) skills, and ability to work efficiently both independently as well as in a collaborative environment
Meticulous record keeping and attention to details
Ability to organize/prioritize work and meet deadlines in the face of multiple and competing demands
Experience in tissue culture (especially of muscle cell lines), histology, molecular biology and biochemistry methods (e.g., RNA, DNA and protein assays) and genetics (managing genetic models) a plus |
| Novartis Oncology |
na |
MA |
11/20/2009
|
| Research Associate - Bacteriology/Biochemistry |
| The ideal candidate will have a BSc/MSc degree in molecular biology or biochemistry and several years of relevant industry experience within an infectious diseases context. |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Research Associate |
| See above |
| 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 |
| Biogen Idec, Inc. |
Washington DC |
DC |
11/20/2009
|
| Research & Support Analyst, Government Relations |
| 3-5+ years of previous relevant and related experience |
| BD (Becton, Dickinson and Company) |
Mebane |
NC |
11/20/2009
|
| Research & Development Validation Engineer II |
| See above |
| 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. |
| BD (Becton, Dickinson and Company) |
San Jose |
CA |
11/20/2009
|
| Reliability Engineer II |
| See above |
| 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
|
| 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. |
| Vertex Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Regulatory Project Manager |
| PREFERRED EDUCATION AND EXPERIENCE:
BS or BA is required. A minimum of 5 years experience in an FDA-regulated industry is required including a minimum of 3 years project management experience.
Vertex Pharmaceuticals |
| BD (Becton, Dickinson and Company) |
Sandy |
UT |
11/20/2009
|
| Regulatory Compliance Complaint Analyst |
| See above |
| Vertex Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| Regulatory CMC Manager |
| ? Demonstrates expert knowledge of FDA regulations, guidelines, and precedents related to drug product development, including Quality by Design (QbD) initiatives
? Knowledge of EU, Canada and ROW regulations, guidelines and precedents
? Proven ability to impact team decision making
? Ability to communicate with all levels within the company and can act as liaison / representative both internally and externally
? Exhibits project management skills necessary to perform complex tasks independently and work on multiple projects simultaneously
? Has a proven track record of successful interaction with regulatory authorities and in preparation of major regulatory submissions
? M.S. (or equivalent degree) and 4+ years of relevant work experience
? B.S. (or equivalent degree) and 6+ years of relevant work experience
Vertex Pharmaceuticals Incorporated is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company's strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Vertex's product pipeline is focused on viral diseases, cystic fibrosis, inflammation, autoimmune diseases, cancer, and pain. Vertex co-discovered the HIV protease inhibitor, Lexiva, with GlaxoSmithKline.
Vertex Pharmaceuticals |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Regulatory CMC Liaison / Biologics |
| Minimum:
Relevant scientific degree in biotechnology, biochemistry and cell biology or equivalent.
Languages:
Fluent English required (oral & written).
Experience / Professional Requirements:
? Several years of experience in regulatory preferred.
? Excellent working knowledge/experience in regulatory submissions and approval processes for Biopharmaceuticals and ability to deal with complex CMC regulatory issues and requirements
? Strong background in biopharmaceutical development (e.g. cell culture, downstream processing, analytics). Biologics experience desired
? Proven track record in successfully leading/working in interdisciplinary teams, and of planning, coordinating and leading activities simultaneously on multiple projects.
? Strong interpersonal, organizational, communication, presentation, negotiation and problem solving skills. |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Regulatory Affairs Specialist |
| See above |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
11/20/2009
|
| Regulatory Affairs Specialist |
| See above |
| 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
|
| 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. |
| Novartis Oncology |
na |
HI |
11/20/2009
|
| Regl Scientific Mgr/Dir (Hawaii) |
| Position will be filled at level commensurate with experience:
Advanced scientific degree (MD, PhD, or PharmD) with a minimum of 3 years of Postdoctoral experience in the pharmaceutical industry (preferred) or other healthcare/ managed markets environment.
Field-based medical and/or managed care with teaching experience preferred. Thorough knowledge of clinical medicine, managed markets, pharmacoeconomics, disease management, and medical research. Thorough knowledge of medicine (including pharmacotherapy), treatment guidelines, clinical research processes, customer strategies, and FDA promotional guidelines, regulations, and ethical guidelines applied to the pharmaceutical industry is preferred. Excellent interpersonal communication and presentation skills are required. Ability to network and partner with important customers, including thought leaders, large group practices, medical directors, and pharmacy directors is required. Must be science-oriented and be able to prioritize and work effectively in a constantly changing environment. Must have the ability to gain customer feedback, uncover business opportunities for Novartis and pair customer's unmet needs with available internal resources. Active membership in professional society(ies) is a plus. Working knowledge of Microsoft Office Suite (Word, PowerPoint, and Excel) and associated hardware is required. Must be a strong team player and effectively interface with other internal departments, including Corporate Customers, Regional Operating Units, Marketing, Sales, New Product Commercialization, Medical Affairs, Research, and Business Analysis. The RSM/D position is associated with approximately 60% travel. Salary flexible. |
| Novartis Oncology |
na |
UT |
11/20/2009
|
| Regl Account Scientific Asc Dir/Director (AZ, CO, NM, NV and UT) |
| Position will be filled at level commensurate with experience.
MD, PharmD, or PhD with 4 years Post-Doctoral experience required. Field-based medical and/or managed care experience preferred. Thorough knowledge of clinical medicine, managed markets, pharmacoeconomics, disease management, and medical research. Excellent interpersonal communication and presentation skills, (including ability to network), strong personal integrity, teamwork abilities and a customer focus are necessary. Must possess a thorough understanding of the FDA, OIG, HIPAA, and GCP/ICH guidelines relevant to the pharmaceutical industry. Must be able to organize, prioritize, and work effectively in a constantly changing environment. Active membership in professional society(ies) is a plus. Working knowledge of Microsoft Office Suite (Word, PowerPoint, and Excel) and associated hardware is required. Ability to interface effectively with a variety of technical platforms for the collection, review, and dissemination of medical information. Demonstrated record of scientific/medical publication. Demonstrated knowledge of GCP practices and standards. Demonstrated technical expertise in at least one disease or therapeutic area. The RASM/D position is associated with approximately 60% travel. Salary flexible. |
| AstraZeneca Pharmaceuticals |
New York City |
NY |
11/19/2009
|
| Regional Sales Specialist |
| Requirements:
- A bachelor?s degree (upon hire)
- Valid drivers license and a safe driving record.
Preferred:
- Cumulative GPA of 3.0 or higher
- Previous leadership experience
- Strong communication, presentation, and project management skills
|
| 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 |
| Novartis Oncology |
na |
NJ |
11/20/2009
|
| Regional Associate Director US Clinical Operations, Oncology |
| ? BS degree in a scientific or health care discipline.
? Expert in Oncology with established contacts in the medical community
desired
? Demonstrated skill sets, competency, and proficiency in clinical research
and relevant people management skills.
? Thorough understanding of international aspects of the drug development
process
? Extensive knowledge of GCP/ICH, FDA, local regulations, and trial
monitoring practices
? Matrix management skills in a local and global environment
? Excellent writing, oral and interpersonal communication skills as well as
strong organizational skills
? Proficiency in relevant computer software applications
? Ability to travel a minimum of 50%
? Ability to interact/communicate in matrix organization.
? At least 6 years experience in clinical research.
? At least 2 years supervisory experience is preferred.
? At least 5 years monitoring experience is preferred.
? Experience in project management a Plus
? Strong computer knowledge in Word, PowerPoint, Excel and Lotus Notes
At least 6 years |
| Millennium Pharmaceuticals |
Cambridge |
MA |
11/19/2009
|
| REGIONAL ACCOUNT MANAGER- SouthEast (FL, PR, GA,AL) |
|
| BD (Becton, Dickinson and Company) |
Mebane |
NC |
11/20/2009
|
| Receiving Associate II |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| Rebate Reconciliation Associate |
| 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) |
Baltimore |
MD |
11/20/2009
|
| R&D Sr. Optical Engineer |
| See above |
| Agilent Technologies, Inc. US |
Loveland |
CO |
11/20/2009
|
| R&D Software Intern |
| Qualifications:
Completion of junior year at an accredited 4- year university working toward a degree in Electrical Engineering, Computer Engineering or Computer Science.
? Working knowledge of C++.
? Knowledge of objected oriented programming concepts and design.
? The ability to work in a team and across geographic boundaries.
? Good verbal and written communication skills.
cb~11/14/2009 |
| Agilent Technologies, Inc. US |
Colorado Springs |
CO |
11/20/2009
|
| R&D Software Engineer |
| Position requires:
? BS/MS Degree in Computer Science or equivalent and a minimum of 5+ years SW development experience
? 5+ yrs Java Development
? Experience building devkits is preferred
? C++ experience desirable
? Linux OS experience desirable
? Telecom or general networking industry knowledge is helpful ( as related to network quality of service)
? Experience with WEB application development
? Knowledge of FLEX GUI Builder, REST API, and XML/XSD, GUI human factors background is an added plus
? Excellent verbal and written communication skills
? Ability to work with cross-functional global teams
? Results-oriented and track record of success in delivering to critical project deadlines
? Strong sense of initiative and ability to work autonomously
These additional skills are strongly preferred:
? Experience with Object and data modeling
? Web based transactions (managing sessions, persistence of the data, JPA)
~cb~8/27/2009 |
| Agilent Technologies, Inc. US |
Colorado Springs |
CO |
11/20/2009
|
| R&D Software Engineer |
| Position requires:
? BS/MS Degree in Computer Science or equivalent and a minimum of 5+ years SW development experience
? 5+ yrs Java Development
? Linux OS experience
? Telecom or general networking industry knowledge is helpful ( as related to network quality of service)
? Experience with WEB application development
? Knowledge of FLEX GUI Builder, REST API, and XML/XSD, GUI human factors background is an added plus
? Excellent verbal and written communication skills
? Ability to work with cross-functional global teams
? Results-oriented and track record of success in delivering to critical project deadlines
? Strong sense of initiative and ability to work autonomously
These additional skills are strongly preferred:
? Experience with Object and data modeling
? Web based transactions (managing sessions, persistence of the data, JPA) |
| Agilent Technologies, Inc. US |
Colorado Springs |
CO |
11/20/2009
|
| R&D Software Engineer |
| Position requires:
? BS/MS Degree in Computer Science or equivalent and a minimum of 5+ years SW development experience
? 5+ yrs Java Development, with a significant portion of this in the client server area.
? Experience with Object and data modeling
? Experience with WEB application development
? Experience creating UI?s using FLEX Builder.
? Experience working with XML and XSD?s.
? Experience with database access and database design.
? Excellent verbal and written communication skills
? Ability to work with cross-functional global teams
? Results-oriented and track record of success in delivering to critical project deadlines
? Strong sense of initiative and ability to work autonomously
These additional skills are strongly preferred:
? Network protocol knowledge and experience
? Experience with multi-threaded transaction systems
? Linux OS experience
? Telecom or general networking industry knowledge is helpful ( as related to network quality of service)
? Web based transactions (managing sessions, persistence of the data, JPA)
? Knowledge of, REST API, GUI human factors background is an added plus
? C++ programming
? Prefer experience will some or all of the following: JUnit, MySql, Hibernate, JMS, XML and Java parsers, J2EE, JTA, JMX, Java Patterns.
~cb~8/18/2009 |
| Agilent Technologies, Inc. US |
Colorado Springs |
CO |
11/20/2009
|
| R&D Software Engineer |
| Position requires:
? BS/MS Degree in Computer Science or Human Factors Engineering or HCI with a minimum of 5+ years experience working as a Human Factors Engineer on software products
? Experience with User Interface Design and Usability is a must
? Experience developing User Interface software is a must.
? Expertise in HCI/UI/Usability standards and de-facto standards is preferred
? Excellent verbal and written communication skills
? Ability to work with cross-functional global teams
? Results-oriented and track record of success in delivering to critical project deadlines
? Strong sense of initiative and ability to work autonomously |
| Agilent Technologies, Inc. US |
Colorado Springs |
CO |
11/20/2009
|
| R&D Network Engineer |
| This role requires a well rounded, hands-on Network Engineer who will function as a Network expert, Software development engineer, and Test Engineer. The individual must possess a BS Engineering ( or equivalent) and possess advanced knowledge in a high-performance datacenter with direct support and network services engineering responsibilities. Network certifications are strongly preferred. C++ and XML Software development skills are also strongly preferred. Other key skills:
? Advanced experience with configuration and support of Cisco routers and switches (minimum 7+ years)
1.Desired Cisco hardware knowledge with platforms 6500, 7500, 4500, 3800, 3700, 2900
? Advanced experience with configuration and support of Hewlett Packard switches (minimum 5+ years)
1.Desired Hewlett Packard knowledge with platforms Procurve 4000m/8000m, 3400, 3500, 5300, 5400
2.Advanced experience with configuration and support of Juniper equipment.
3. Advanced experience with configuration and support of Alcatel-Lucent equipment.
? Strong layer 2 and layer 3 experience with a focus on enterprise and data center switching and routing including: Ethernet, Spanning Tree, VLAN, MPLS, Link Aggregation, ether-channel, QoS, 802.1Q, DHCP, ARP, RARP, IGMP, SNMP, IPv4, VoIP, multicast routing protocols, 10 Gig Ethernet, minimum 5 years
? Demonstrated ability to gather design requirements or problem requirements and recreate infrastructure so that initial design validation can be completed or in the case of a problem being able to troubleshoot and isolate root cause.
? In-depth knowledge of network element infrastructure, error reporting, OS limitations, etc.
? Strong Customer interface skills
? Excellent written and communication skills
? Experience in mentoring peers and junior level engineers and administrators
~cb~8/31/2009 |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
11/20/2009
|
| R&D Mechanical Project Engineer |
| See above |
| Agilent Technologies, Inc. US |
Colorado Springs |
CO |
11/20/2009
|
| R&D Mechanical Engineer - Intern |
| - Bachelors Degree or Masters Degree in ME in progress with a Graduation Date of May 2011 to May 2012.
- Experience via course work or previous internships
- Strong written and verbal communication skills.
- Excellent teamwork skills.
- Self-starter. Willing and able to quickly learn new technologies.
cb~10/27/2009 |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| R&D Manager, Technology Development |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| R&D Manager, Packaging Technology |
| See above |
| BD (Becton, Dickinson and Company) |
Sandy |
UT |
11/20/2009
|
| R&D Manager, Infusion Systems |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| R&D Manager, Emerging Markets |
| See above |
| 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 |
| BD (Becton, Dickinson and Company) |
Baltimore |
MD |
11/20/2009
|
| R&D Electrical Project Engineer |
| See above |
| Agilent Technologies, Inc. US |
Colorado Springs |
CO |
11/20/2009
|
| R&D Electrical Engineer - Intern |
| - Bachelors Degree or Masters Degree in EE in progress with a Graduation Date of May 2011 to May 2012.
- Experience via course work or previous internships
- Strong written and verbal communication skills.
- Excellent teamwork skills.
- Self-starter. Willing and able to quickly learn new technologies.
cb~10/27/2009 |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| R&D Director, Preanalytical Systems |
| See above |
| BD (Becton, Dickinson and Company) |
Franklin Lakes |
NJ |
11/20/2009
|
| R&D Director, Additive and Chemistry |
| See above |
| Johnson & Johnson Family of Companies |
|
NJ |
11/19/2009
|
| R&D Co-Op- Fall 2010 |
| Candidates must be working towards a B.S., M.S., or PhD degree in Chemical Engineering, Materials (Science) Engineering, Biological or Biomedical Engineering, Biology, Chemistry, Pharmaceutical Sciences, or other related concentration. Candidates must possess a 3.0 GPA or higher. Candidates must be authorized to work in the U.S. for any employer. |
| 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 |
| Johnson & Johnson Family of Companies |
Bridgewater |
MA |
11/19/2009
|
| Quality Technician II (2 of 2) |
| A minimum of a High School diploma or equivalent required. A minimum of 1 year of inspection experience in a precision machining and/or casting environment required. Medical Device inspection experience preferred. Blue print interpretation skills and a working knowledge of GD&T (Geometric Dimensioning and Tolerancing) applications required. Working knowledge of various applications of shop mathematics is preferred. Working knowledge of CMM (Coordinate Measurement Machine) inspection and programming is a plus. CMM experience on Brown & Sharpe MM4 and/or with PC-DMIS is a plus. Excellent written, oral communication, organization and computer skills will be needed. ASQ Certification is a plus. Optical Comparators experience or exposure is required. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! |
| BD (Becton, Dickinson and Company) |
Wilson |
NC |
11/20/2009
|
| Quality Systems Leader |
| See above |
| Johnson & Johnson Family of Companies |
Cincinnati |
OH |
11/19/2009
|
| Quality Systems and Compliance Specialist |
| Minimum of a BS or BA in Business, applied Sciences, Quality or an Engineering-related discipline or equivalent work experience is required. CQA certification is strongly preferred. CQE and/or CRE Certification is also preferred. A minimum of 7+ years of total work experience in Regulatory Affairs and/or Quality Assurance in a medical device or pharmaceutical environment is required. Strong auditing skills are required. Experience managing or participating in internal audit programs is also required. Strong Project Management skills, excellent verbal and written communication skills, influencing management skills are required. Knowledge of ISO-GMPs is required. Knowledge of GLP, GCP Quality Systems and international requirements is preferred. Knowledge of design and development, labeling and manufacturing systems is required. Knowledge of continuous improvement principles is preferred. Experience and/or interactions with a Regulatory agency is preferred. If you want to explore the many small-company environments behind the big-company impact of the Johnson & Johnson Family of Companies, bid on this position today! Johnson & Johnson is committed to diversity and invites all interested candidates to apply for positions of interest. EOE M/F/D/V Please note: In order to be considered eligible for an interview, candidates must apply online through the appropriate web portal. |
| BD (Becton, Dickinson and Company) |
Burlington |
NC |
11/20/2009
|
| Quality Engineer II, Reagents |
| See above |
| 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 require | |
