Onsite Document Control Specialist – GMP/Quality
Listed on 2026-10-17
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Quality Assurance - QA/QC
Regulatory Compliance Specialist, Production QC/QA, Quality Control - QC Analysts/Managers, QA Specialist - Analyst/Manager
MADE Scientific Inc. in Princeton, NJ is seeking a Document Control Specialist to manage GMP and quality documentation, ensuring audit readiness. The role requires strong organization, attention to detail, and collaboration across teams to maintain confidential, compliant records in a regulated environment.
The position is full-time and on-site in Princeton, offering opportunities to support internal audits and continuous improvement of document workflows within a CDMO setting.
We are looking to fill the Onsite Document Control Specialist – GMP/Quality position at MADE Scientific Inc in Princeton, NJ, United States.
This opening is for the Onsite Document Control Specialist – GMP/Quality role at MADE Scientific Inc.
We are seeking a motivated Onsite Document Control Specialist – GMP/Quality to join MADE Scientific Inc in Princeton, NJ, United States.
Consider building your career as a Onsite Document Control Specialist – GMP/Quality at MADE Scientific Inc.
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