What are the responsibilities and job description for the QC Deviations Specialist position at Commissioning Partners?
QC Deviations Specialist
Newark, NJ
Competitive pay
3 years of experience in regulated manufacturing environment
Overview:
Our client in NJ is seeking a QC Deviations Specialist with 3 years of experience in pharma manufacturing or QC labs.
What You’ll Work On:
- Investigate QC laboratory deviations
- Perform Root Cause Analysis (RCA) and support CAPA development
- Write clear, compliant deviation reports
- Support OOS / OOT investigations
- Review analytical data for accuracy & GMP compliance
- Ensure adherence to Data Integrity & regulatory standards
- Collaborate with QC, QA, and Manufacturing teams
- Maintain audit-ready documentation
Who We’re Looking For:
- Strong understanding of GMP, QC workflows, and deviation management
- Experience with CAPA systems and laboratory investigations
- Excellent communication & documentation skills