Floor QA Specialist - GMP, Sacramento | Eligible
Listed on 2026-10-07
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Quality Assurance - QA/QC
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Pharmaceutical
Nivagen Pharmaceuticals is seeking an In Process QA Specialist in Sacramento to ensure pharmaceutical products meet quality standards during manufacturing. You will monitor, sample, test, and document processes to maintain GMP and regulatory compliance.
Responsibilities include line clearances, in-process checks, document review, and supporting deviation investigations with CAPA development. Collaboration with Manufacturing and QA teams is essential to drive continuous improvement.
This posting is for the On-the-Floor QA Specialist - GMP, Sacramento | Bonus Eligible role at Nivagen Pharmaceuticals, based in Sacramento, CA, United States.
The position is based in Sacramento, CA, United States.
This opportunity is part of our work in Bio & Pharmacology & Health, Management & Operations.
The advertised compensation is 70.000 - 90.000.
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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