GMP QA Documentation Specialist - Batch Records
Astrix
Astrix is seeking a QA Specialist II/III for a one-year contract in Vista, CA. The role involves reviewing production batch records and GMP documentation to ensure compliance in a pharmaceutical manufacturing environment. Candidates with a Bachelor's degree and 3-7 years of QA experience are preferred, along with strong attention to detail and organizational skills. This is a critical position to support quality assurance operations. #J-18808-Ljbffr Astrix
Vacancy posted 1 day ago
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