QA Specialist I - cGMP Compliance & SOP Champion
Avecia Pharma
A chez Avecia Pharma, the Quality Assurance Specialist will document and audit cGMP practices across the site, developing and revising QA procedures to strengthen cGMP compliance per USFDA Title 21 CFR Part 210, 211 and ICH Q7 guidance. Key responsibilities include coordinating with departments to meet GMP requirements, approving SOPs, and ensuring batch records and QC docs meet quality standards. The role emphasizes liaison with clients and cross-functional collaboration. #J-18808-Ljbffr Avecia Pharma
Vacancy posted 3 days ago
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