GMP Document Control Specialist — Pharma/Biologics
Planet Pharma
Planet Pharma in Newark, CA seeks a detail-oriented Document Control Specialist to support controlled-document lifecycles across production, testing, validation, and quality operations within a GMP environment. You will collaborate with cross-functional partners, maintain templates, and ensure timely, accurate documentation. The role emphasizes strong organizational skills, proficiency with Word/Excel/Acrobat/Visio, and experience with electronic document management systems like Veeva #J-18808-Ljbffr Planet Pharma
Vacancy posted 2 days ago
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