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Documentation Specialist I: GMP Records & CAPA

Aequor Inc

Aequor is seeking candidates for a role focused on reviewing manufacturing batch records to ensure compliance with regulatory requirements. Candidates with experience in CAPA, technical writing, and the pharmaceutical or biotech industry are preferred. This position offers a contract until December 2026 with the potential for extension. Applicants must be detail-oriented, work accurately, and thrive in a team environment. #J-18808-Ljbffr

Vacancy posted 2 days ago
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