GMP QA Specialist (Level I-III) - Pharma Manufacturing
Actalent
Actalent is seeking a detail-oriented Quality Assurance Specialist to support operations in a GMP-regulated pharmaceutical manufacturing environment in San Diego, CA. This role provides growth opportunities (Level I–III) based on experience and strong exposure in a fast-paced production setting. The ideal candidate will have a Bachelor's degree and QA experience in a GMP environment. Responsibilities include reviewing production records and performing document control activities. #J-18808-Ljbffr Actalent
Vacancy posted 4 days ago
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