Document Control Specialist — cGMP QA
Listed on 2026-10-18
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Quality Assurance - QA/QC
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Healthcare
Data Scientist
Rentschler Biopharma SE in Milford, MA is seeking a Documentation Control Specialist to manage and verify records in our Quality group, ensuring compliance with regulatory requirements and cGMP standards.
You will issue, reconcile, and archive logbooks and batch records, support inspections and audits, and help maintain a robust electronic quality management system using Master Control. Strong attention to detail and teamwork are essential.
Step into the Document Control Specialist I — cGMP QA role at Rentschler Biopharma SE in Milford, MA, United States and grow with us.
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
Learn more about the Document Control Specialist I — cGMP QA role in the description above.
We appreciate your interest in this position.
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