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Sr or Validation or FDA or GMP jobs in Columbus, OH, 43215

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Job alert Jobs 1 - 10 of 634

Sr Computer System Validation (CSV) Engineer

Forge Biologics  –  Columbus, OH
... About The Role We are currently seeking a Sr Computer Systems Validation (CSV) Engineer to join the Forge Biologics team, a ... Their focus will be on computerized systems in support of Forges applications and GMP equipment. Forge provides and ... - Apr 17

Associate Manager, GMP Maintenance

Forge Biologics  –  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  –  Columbus, OH
... About The Role We are currently seeking a Sr Computer Systems Validation (CSV) Engineer to join the Forge Biologics team, a ... Their focus will be on computerized systems in support of Forges applications and GMP equipment. Forge provides and ... - Apr 18

Associate Director, Manufacturing (GMP)

Amplifybio, LLC  –  New Albany, OH, 43054
... AmplifyBio is seeking to hire a (Sr.) Manager/Associate Director of Manufacturing to join our growing team! The (Sr.) ... GMP Compliance: Oversee all manufacturing activities to ensure compliance with GMP regulations, FDA guidelines, and industry ... - Apr 24

Associate Scientist I, GMP Manufacturing - Downstream

Forge Biologics  –  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 25

Associate Manager, GMP Maintenance

Forge Biologics  –  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  –  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

CQV Engineer / Validation Engineer

Verista  –  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

Materials Handler (GMP)

Amplifybio, LLC  –  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. ... - Mar 29

Associate Scientist I, GMP Manufacturing - Upstream

Forge Biologics  –  Columbus, OH
... About The Team The GMP Manufacturing department is responsible for the manufacturing of AAV Gene Therapy products in accordance with the highest standards of Good Manufacturing Practices (GMPs). This department ensures that the products produced are ... - Apr 19
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