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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 ingredients2/11/2014 Watertown, MA Save This Job
Job Code: 005-13-07 Location: Rockville, MD Applicants must meet the following requirements: Bachelor?s or Master?s degree in biology, biotechnology or related scientific discipline Minimum of 2 years of relative industry experience Knowledge of cell culture methods, good1/27/2014 Rockville, MD Save This Job
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 for2/19/2014 Durham, NC Save This Job
Main areas of responsibility include working with a team of Manufacturing Associates on process preparations and process execution tasks to include: Responsible for operating various Cell Culture equipment that include; Bioreactors, NOVA Flex, Vi-Cell and Microbial equipment that2/19/2014 Durham, NC Save This Job
Assist in execution of procedures for cell culture manufacturing, purification, or support area of manufacturing using SOP?s and batch records. Responsible for various duties that are required to produce product including but not limited to cell expansion; cell feeding,1/20/2014 Durham, NC Save This Job
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 The2/26/2014 Rockville, MD Save This Job
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 chromatographic2/26/2014 Rockville, MD Save This Job
Job Summary The ideal AD, Quality Assurance candidate is a technical savvy quality professional with prior management experience. This position is responsible for a number of key quality systems and close oversight of CMOs. The job requires up to 10% travel, excellent1/27/2014 Palo Alto, CA Save This Job
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 new1/13/2014 Philadelphia, PA Save This Job
Description Demonstrates understanding and application of the technology encompassed in and practiced with the Singulex assays as well as basic immunoassay principles in planning and executing experiments. Performs assays and data analysis with moderate supervision. Operates lab2/17/2014 Alameda, CA Save This Job
Description: This individual will support pre-approval compounds in the development phase through marketing registration and post approval follow up. Responsible for implementation of practical, workable plans to support all CMC regulatory filings. Oversees and participates in12/31/2013 San Francisco, CA Save This Job
Department: CMC Job Title: Laboratory Support Assistant Reports To: Director, Radiochemistry and Radiopharmaceutical Development Description: Avid Radiopharmaceuticals, Inc. (Avid RP), a wholly owned subsidiary of Eli Lilly and Company, is a molecular imaging company1/13/2014 Philadelphia, PA Save This Job
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 and1/13/2014 Philadelphia, PA Save This Job