GMP Quality Documentation Specialist I
Actalent
Actalent is seeking a Quality Specialist I based in Columbus, OH. This role serves as a crucial first line of defense for quality laboratories, focusing on documentation and compliance rather than hands-on lab work. The Quality Specialist will operate within a Quality Management System to support the manufacture of phase-appropriate material in a state-of-the-art facility. The ideal candidate will have a Bachelor’s degree in Biology or a related field and experience in regulated environments. Responsibilities include ensuring documentation and product sample management in compliance with regulatory standards. #J-18808-Ljbffr Actalent
Vacancy posted 3 days ago
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