| Job alert | Jobs 11 - 20 of 1095 |
Sr Computer System Validation (CSV) Engineer
Forge Biologics
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Columbus, OH
... in partnership with functional teams, ensuring the documentation meets regulatory requirements and quality standards. ... for Pharmaceutical Engineering (ISPE) guidelines such as GAMP 5, FDA Data Integrity guidelines, 21 CFR Part 11 and Annex 11 ... - May 01
Quality Assurance Manager
T. Marzetti Company
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Columbus, OH
... preferred: Preventive Controls Qualified Individual (PCQI), HACCP (16-Hour), Internal Auditor Training (FSSC22000/ISO, BRC) Prior experience handling third-party audits, customer audits, and regulatory inspections (FDA/USDA) strongly preferred. ... - May 02
Associate Director, Manufacturing (GMP)
Amplifybio, LLC
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New Albany, OH, 43054
... FDA guidelines, and industry standards specific to cell and gene therapy. Adhere to robust quality systems, including batch record review, deviation management, and change control processes, to ensure regulatory compliance and product quality. ... - May 02
Associate, Research Operations - QC
Sarepta Therapeutics
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Columbus, OH
... The candidate will have a clear understanding of the data capture process and will perform QC review of gene therapy research data under direct supervision. The candidate will assist with tracking, trending, and reporting results. The candidate will ... - Apr 06
Mechanical Equipment Engineer
ACL Digital
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New Albany, OH, 43054
... You will evaluate and determine if process equipment maintenance, and technical cleaning systems are maintained in compliance with all applicable industry standards, regulatory standards and FDA standards in the Inspection and Packaging area. ... - Apr 20
Associate Director, Manufacturing (GMP)
Amplifybio, LLC
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New Albany, OH, 43054
... FDA guidelines, and industry standards specific to cell and gene therapy. Adhere to robust quality systems, including batch record review, deviation management, and change control processes, to ensure regulatory compliance and product quality. ... - May 02
Medical Safety Reviewer
DivIHN Integration Inc
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Columbus, OH
... - the investigation and reporting of medical product experiences, in-depth investigation of medical adverse events and works with Medical Affairs, Clinical, and Regulatory Affairs in the preparation of documentation on adverse events for the FDA; ... - May 03
Sr Computer System Validation (CSV) Engineer
Forge Biologics
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Columbus, OH
... in partnership with functional teams, ensuring the documentation meets regulatory requirements and quality standards. ... for Pharmaceutical Engineering (ISPE) guidelines such as GAMP 5, FDA Data Integrity guidelines, 21 CFR Part 11 and Annex 11 ... - Apr 18
Production Specialist, Hospital Services (Full-Time, 1st Shift)
Versiti, Inc.
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Columbus, OH
... regulatory and operational standards as specified in the Standard Operating Procedures and departmental procedures. ... products Performs and documents equipment function checks and QC as required Maintains a level of productivity that allows ... - Apr 26
Associate Director, Manufacturing (GMP)
Amplifybio, LLC
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New Albany, OH, 43054
... FDA guidelines, and industry standards specific to cell and gene therapy. Adhere to robust quality systems, including batch record review, deviation management, and change control processes, to ensure regulatory compliance and product quality. ... - May 02