Onsite Quality Document Control Specialist
Tandym-Group
Tandym-Group is assisting a biotech client in Bedford, MA to hire a Document Control Specialist - Quality to manage controlled documents and archival within a GxP environment. The role focuses on SOP adherence, document reconciliation, and preparation for audits, with a Monday–Friday onsite schedule. A B.S. in science/engineering and 1–4 years in pharma/biotech quality are required, plus proficiency with Excel, Word and PowerPoint. #J-18808-Ljbffr Tandym-Group
Vacancy posted 1 day ago
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