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GMP Technical Writer: Pharma Documentation Specialist
Job in
Springfield, Union County, New Jersey, 07081, USA
Listed on 2026-07-07
Listing for:
CeDent
Full Time
position Listed on 2026-07-07
Job specializations:
-
Pharmaceutical
Pharmaceutical Manufacturing
Job Description & How to Apply Below
CeDent, located in Springfield, New Jersey, is looking for a detail-oriented GMP Pharmaceutical Technical Writer. The role involves creating and maintaining controlled documentation in compliance with Good Manufacturing Practices. Candidates should have a Bachelor's degree in a relevant field and at least 2 years of experience in a GMP-regulated environment.
The Technical Writer will work closely with cross-functional teams, ensuring clarity and accuracy in documentation essential for pharmaceutical manufacturing and regulatory processes.
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