GMP Quality Systems Specialist: Documentation & Compliance
Actalent
Actalent is seeking a Quality Systems Specialist in San Diego, CA to support quality assurance operations in a GMP-regulated pharmaceutical environment. This role involves reviewing batch records, compliance documentation, and supporting production activities to ensure quality standards are met. The ideal candidate will have a Bachelor's degree in a relevant field and 2-5+ years of experience within quality assurance. Responsibilities will scale based on experience level, and the position offers a fully onsite work environment. #J-18808-Ljbffr Actalent
Vacancy posted 2 days ago
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