Centralized Document Management Team (CDMT) Specialist

The role is part of Pfizer's Centralized Document Management Team at the Kalamazoo site, responsible for end‑to‑end lifecycle management of GMP documents using QualityDocs. The incumbent will author, review, and manage SOPs, batch records, and other regulated documents, ensure compliance with cGMP and data‑integrity standards, and support inspection readiness and continuous improvement initiatives.