QA/QMS Senior: Deviations & Investigations Lead
Listed on 2026-10-06
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Quality Assurance - QA/QC
Regulatory Compliance Specialist -
Pharmaceutical
Regulatory Compliance Specialist
Nivagen Pharmaceuticals is seeking a QA/QMS Senior Specialist to lead deviations and investigations for sterile GMP manufacturing. You will own the lifecycle from initiation to closure, perform root cause analyses, and ensure FDA/cGMP compliance while coordinating across QA, QC, Engineering, and Validation teams.
The role requires strong investigative skills, technical writing ability, and experience with Track Wise or similar QMS systems, aiding inspection readiness and process improvements.
The QA/QMS Senior:
Deviations & Investigations Lead role at Nivagen Pharmaceuticals is now open for applications in Sacramento, CA, United States.
For the QA/QMS Senior:
Deviations & Investigations Lead position at Nivagen Pharmaceuticals, we are reviewing applications now.
Step into the QA/QMS Senior:
Deviations & Investigations Lead role at Nivagen Pharmaceuticals in Sacramento, CA, United States and grow with us.
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