GMP Manufacturing Associate Jobs

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GLP/GMP Quality Associate III

EnVivo Pharmaceuticals

Reporting to the Senior Manager of Quality Assurance, Good Laboratory Practices (GLP) & current Good Manufacturing Practices (cGMP), the GLP/GMP Quality Associate will perform documentation reviews associated with the QA review and release of active pharmaceutical ingredients

2/17/2014  Watertown, MA  Save This Job

Manufacturing Associate (Protein Purification) (14-482)


Job Code: 14-482 Location: Rockville, MD Applicants must meet the following requirements: Bachelor?s or Master?s degree in life sciences or related scientific discipline 1-5 years of experience in a GMP manufacturing facility Sound understanding of protein purification

4/3/2014  Rockville, MD  Save This Job

Manufacturing Associate, Upstream

KBI Biopharma

Main areas of responsibility include working with a team of Manufacturing Associates on process preparations and process execution tasks to include: Perform weight-outs, measurements, counts and document activities to obtain raw materials and intermediates required for

2/24/2014  Durham, NC  Save This Job

Associate Manager, Document Control (014-14-01)


Applicants must meet the following requirements: Bachelor?s Degree or equivalent in life science or engineering field with 7 years related experience in GMP manufacturing environment, including 4 years GLP archivist experience Knowledge of U.S. and E.U. GMP regulations The

3/4/2014  Rockville, MD  Save This Job

Bioprocess Associate III (025-14-01)


Job Code: 025-14-01 Location: Rockville, MD Applicants must meet the following requirements: Bachelor?s Degree or equivalent in biochemistry or related scientific discipline with 5 years relevant experience in biopharmaceutical development, including chromatographic

3/4/2014  Rockville, MD  Save This Job

Senior Manager/Associate Director, Quality Assurance (14-119)


Description: FibroGen seeks a Quality Assurance Senior Manager/Associate Director to support the manufacture of Drug Substance and Drug Product at Contract Manufacturing Organizations (CMO) and Contract Research Organizations (CRO) to ensure FibroGen products are in compliance

4/15/2014  San Francisco, CA  Save This Job

Senior Manager/Associate Director, Validation (14-555)


Job Code: 14-555 Location: Rockville, MD Applicants must meet the following requirements: Bachelor's degree in a scientific, technical or engineering discipline with a minimum of 10 years experience in a GMP, biotech environment Hands-on experience with writing Validation

4/3/2014  Rockville, MD  Save This Job

Technology Transfer Associate

Avid Radiopharmaceuticals

Department: CMC Job Title: Technology Transfer Associate Reports To: Assistant Director Technology Transfer and CMC Regulations Description: Position Overview: The Technology Transfer Associate will play a key role in the process of technology transfer and setting up new

2/18/2014  Philadelphia, PA  Save This Job

Technical Field Specialist

Avid Radiopharmaceuticals

Reports To: Associate Director, Amyvid US Manufacturing Description: ?Become fully conversant in Avid radiopharmaceutical manufacturing and analytical procedures ?Visit contract manufacturing organization facilities to observe production and testing of Avid products and

2/18/2014  Philadelphia, PA  Save This Job