| Job alert | Jobs 1 - 10 of 727 |
Associate Manager, GMP Maintenance
Forge Biologics
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Columbus, OH
... About The Role: The Associate Manager of GMP Mechanical Maintenance is responsible for the overall preventative, predictive ... Preferred: Experience in documentation management within a structured Quality System (ISO, FDA). Work Environment and ... - Apr 01
Sr Computer System Validation (CSV) Engineer
Forge Biologics
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Columbus, OH
... (PQ) Traceability Matrix (TM) Validation Summary Report Data Integrity/Part 11 testing Support GMP Manufacturing and ... for Pharmaceutical Engineering (ISPE) guidelines such as GAMP 5, FDA Data Integrity guidelines, 21 CFR Part 11 and Annex 11 ... - Apr 17
Associate Director, Manufacturing (GMP)
Amplifybio, LLC
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New Albany, OH, 43054
... GMP Compliance: Oversee all manufacturing activities to ensure compliance with GMP regulations, FDA guidelines, and industry ... new cell and gene therapy products from development to manufacturing, ensuring successful scale-up and process validation. ... - Apr 26
Technician I, GMP Manufacturing - Downstream
Forge Biologics
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Columbus, OH
... About The Role As a Technician I, GMP Manufacturing - Downstream you will play a vital role in the production and ... Assist in the execution of process validation and technology transfer activities, collaborating with cross-functional teams ... - Apr 26
Associate Director, Manufacturing (GMP)
Amplifybio, LLC
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New Albany, OH, 43054
... GMP Compliance: Oversee all manufacturing activities to ensure compliance with GMP regulations, FDA guidelines, and industry ... new cell and gene therapy products from development to manufacturing, ensuring successful scale-up and process validation. ... - Apr 24
Associate Manager, GMP Maintenance
Forge Biologics
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Columbus, OH
... About The Role: The Associate Manager of GMP Mechanical Maintenance is responsible for the overall preventative, predictive ... Preferred: Experience in documentation management within a structured Quality System (ISO, FDA). Work Environment and ... - Mar 29
CQV Engineer / Validation Engineer
Verista
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Columbus, OH
... Resource will be required to draft validation and commissioning documentation including, change requests, system impact ... Requirements Experience in GMP regulated environment Proven attention to detail and organization in project work Capable of ... - Apr 05
Sr Computer System Validation (CSV) Engineer
Forge Biologics
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Columbus, OH
... (PQ) Traceability Matrix (TM) Validation Summary Report Data Integrity/Part 11 testing Support GMP Manufacturing and ... for Pharmaceutical Engineering (ISPE) guidelines such as GAMP 5, FDA Data Integrity guidelines, 21 CFR Part 11 and Annex 11 ... - Apr 18
Materials Handler (GMP)
Amplifybio, LLC
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New Albany, OH, 43054
... Practices (cGMP/GDP) in an FDA regulated industry. 2+ years of experience handling GMP materials in biotech/pharmaceuticals industry is strongly preferred. General understanding of sterile technique and comfortability around wet lab environments. ... - Apr 26
CQV Engineer / Validation Engineer
Verista
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Columbus, OH
... Resource will be required to draft validation and commissioning documentation including, change requests, system impact ... Requirements Experience in GMP regulated environment Proven attention to detail and organization in project work Capable of ... - Apr 04