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QA Document Control Associate - Contract - Rockville, MD
Be the backbone of GMP compliance by managing quality documents with precision and care.
Proclinical is seeking a QA Document Control Associate to support quality documentation processes within the Quality Management System (QMS).
Primary Responsibilities:
The successful candidate role focuses on ensuring accuracy, compliance, and effective control of GMP-related documents. You will play a key part in managing document lifecycles, maintaining inventories, and supporting GMP operations.
Skills & Requirements:
The QA Document Control Associate's responsibilities will be:
If you are having difficulty in applying or if you have any questions, please contact Anderson Maldonado at a.maldonado@proclinical.com.
If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.
Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.
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