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.
#J-18808-LjbffrOn-the-Floor QA Specialist - GMP, Sacramento | Bonus Eligible in sacramento at Unknown Company
This position is listed as full time and onsite.