| Job alert | Jobs 1 - 10 of 602 |
Sr Computer System Validation (CSV) Engineer
Forge Biologics
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Columbus, OH
... life cycle (SDLC) for the validation of new systems and changes for existing systems, to assure that all critical systems remain in a validated state. Their focus will be on computerized systems in support of Forges applications and GMP equipment. ... - Apr 17
Associate Scientist I, GMP Manufacturing - Upstream
Forge Biologics
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Columbus, OH
... About The Team The GMP Manufacturing department is responsible for the manufacturing of AAV Gene Therapy products in ... culture expansion, transfection, and harvest steps, according to Standard Operating Procedures (SOPs) and batch records. ... - Apr 19
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 and corrective maintenance strategies of GMP manufacturing, laboratory, and utility equipment in accordance with the OEM ... - Apr 01
Associate Director, Manufacturing (GMP)
Amplifybio, LLC
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New Albany, OH, 43054
... for leading and overseeing the manufacturing operations within a GMP-compliant facility specializing in advanced therapies. ... batch records, and work instructions for the production of cell and gene therapy products. Perform tasks related to drug substance ... - Mar 25
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
Associate Scientist I, GMP Manufacturing - Upstream
Forge Biologics
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Columbus, OH
... About The Team The GMP Manufacturing department is responsible for the manufacturing of AAV Gene Therapy products in ... culture expansion, transfection, and harvest steps, according to Standard Operating Procedures (SOPs) and batch records. ... - Apr 18
Sr Computer System Validation (CSV) Engineer
Forge Biologics
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Columbus, OH
... life cycle (SDLC) for the validation of new systems and changes for existing systems, to assure that all critical systems remain in a validated state. Their focus will be on computerized systems in support of Forges applications and GMP equipment. ... - Apr 18
CQV Engineer / Validation Engineer
Verista
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Columbus, OH, 43224
... 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 17
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
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 and corrective maintenance strategies of GMP manufacturing, laboratory, and utility equipment in accordance with the OEM ... - Mar 29