CSBio in Milpitas, CA seeks a hands-on Quality Assurance Manager to supervise daily QA activities supporting peptide manufacturing and cGMP compliance. You will manage QA staff, review deviations, CAPAs, change controls, training, batch-record review, audits, and inspection readiness.
The role requires 5+ years in QA within regulated manufacturing, including 2+ years in a supervisory capacity, and strong knowledge of FDA/ICH expectations.
#J-18808-LjbffrSenior cGMP QA Manager – Peptide Manufacturing in milpitas at Unknown Company
This position is listed as full time and onsite.