Senior GMP/GLP Quality Systems Audit Lead; Onsite – Northern CA)
Listed on 2026-10-06
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Quality Assurance - QA/QC
The FDA Group is seeking an experienced GMP/GLP & Quality Systems Audit Consultant to conduct a thorough three-day onsite audit of a life sciences testing facility in Northern California. You will assess laboratory operations, quality systems, room classifications, equipment maintenance, and Quality Unit oversight to identify gaps and risks.
The engagement emphasizes practical, risk-based recommendations and a comprehensive audit report, with follow-up audits anticipated to evaluate progress and
This is a great role to take on the Senior GMP/GLP Quality Systems Audit Lead (Onsite – Northern CA) role at The FDA Group.
This opportunity is part of our work in Bio & Pharmacology & Health, Consulting.
The advertised compensation is 150..
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
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