Planet Pharma
From Planet Pharma's careers page
Status: listed on the employer's own careers page when we last checked (daily). Confirm on their site before applying.
In search for a QA Associate-level temp worker, who has about 3-4 years GMP experience in the biotech / cell and gene industry. This person will support:
Document Control & Management: Oversees the end-to-end lifecycle of controlled documents (SOPs, work instructions, forms), ensuring timely drafting, revision, review, approval, and archival.
Logbook Administration: Manages the issuance, tracking, reconciliation, and periodic review of physical and electronic GMP logbooks to maintain audit readiness.
Veeva Vault Workflows: Administers and troubleshoots electronic document and quality workflows within Veeva Vault, acting as a subject matter expert to resolve bottlenecks and support system users.
Training Oversight: Coordinates role-based training assignments, monitors compliance metrics, tracks overdue curricula, and generates audit-ready training reports for department leads.
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