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The Head, PSSM has global responsibilities and is accountable for overseeing and providing strategic direction and operational implementation for all aspects of advancing the small molecule NCE portfolio including chemistry, analytical, ..
Position Title: Analytical Tech Transfer Specialist - Biopharmaceutical
Working Location: Pennsylvania
Employment Status: Full time
Required Experience: 5 years
Required Education: Bachelors
Travel Required: 10%
• Supports ..
Radius HealthRadius Health is an equal opportunity employer. EEO/Disabled Individuals/Veterans. If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send ..
Quality Analyst I, Stability - 2nd Shift
Your tasks and responsibilities
The primary responsibilities of this role, Quality Analyst I,
Stability - 2nd Shift, are to:
Perform standard ..
The GMP Auditor will be responsible for performing Quality System and GMP compliance Audits of Suppliers and Vendors in the Pharmaceutical manufacturing. Compliance with applicable regulatory guidelines and requirements is ..
When you’re part of the team at Thermo Fisher Scientific, you’ll do important work, and you’ll be valued and recognized for your performance. With talented managers and inspiring coworkers ..
ENGINEERING PROJECT MANAGER WITH PHARMACEUTICAL MANUFACTURING
The candidate for this position will be part of Client's Dosage Form Design and Development group working on combination product development, ..
Amgen is a leading global biotechnology company, with a mission to serve patients around the world. As a science-based, patient-focused organization, we discover and develop innovative therapies to treat serious illnesses. ..
Celgene is a global biopharmaceutical company leading the way in medical innovation to help patients live longer, better lives. Our purpose as a company is to discover and develop therapies that ..
job description reflects assignment of essential functions; it does not prescribe or restrict the tasks that may be assigned.
This position will manage, develop, and coordinate federal, state ..
Job Location: Softworld, Waltham, MA, 02454, USA
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ROLE SUMMARY The Technical Development Manager has global accountability for the development of technical information for customer qualification and continuous support of products within the Pfizer CentreOne business. The incumbent will ..
At Abbott, we're committed to helping people live their best possible life through the power of health. For more than 125 years, we've brought new products and technologies to the world ..
The primary purpose of this position is to develop assays and design, plan and execute the qualification, and transfe r of these analytical assays in support of Vaccine materials release and ..
Quality Control Analyst
Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical ..
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Quality Control (QC) Chemist I Pharmaceutical - ICP/MS exp., Irvine, CArnJob Duties and Responsibilities:rnrntPerform and/or assist with analytical testing of raw materials, in-process samples, and finished products.rntUtilize analytical laboratory instrumentation with ..
Job Description Summary: The Director of Analytical and Formulation Sciences (AFS) is a key leadership role, which manages a large team of scientists across two locations in Princeton, NJ and St. ..
... minimum of 12+ years of pharmaceutical laboratory experience required; or Completed ... minimum of 10+ years of pharmaceutical laboratory experience required; or Completed ... minimum of 8 years of..
Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and ..
Description Celgene is a global biopharmaceutical company leading the way in medical innovation to help patients live longer, better lives. Our purpose as a company is to discover and develop therapies ..
The Global Regulatory Lead Development Products (GRL-DP) is responsible for providing strategic vision and innovative scientific and regulatory leadership in defining the global regulatory strategy for assigned projects. The GRL is ..