Night-Shift Manufacturing QA Lead: GMP Compliance
Listed on 2026-10-09
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Quality Assurance - QA/QC
Regulatory Compliance Specialist, Production QC/QA -
Manufacturing / Production
Regulatory Compliance Specialist, Production QC/QA
Novartis is seeking a Manufacturing Quality Assurance Specialist for an onsite, third-shift role in Durham, NC. You will provide hands-on quality oversight across manufacturing processes, review batch records, and lead deviation investigations to ensure regulatory compliance and patient safety.
The role requires a BS in a relevant science, 5+ years in GMP manufacturing, and strong CFR/FDA/EU knowledge. Onsite 11:00 pm–7:30 am shift, with audits and continuous improvement responsibilities.
For the Night-Shift Manufacturing QA Lead: GMP Compliance position at U473 (FCRS = US473) Novartis Innovative Technologies Inc, we are reviewing applications now.
This is a genuine position to take on the Night-Shift Manufacturing QA Lead: GMP Compliance role at U473 (FCRS = US473) Novartis Innovative Technologies Inc.
As a Night-Shift Manufacturing QA Lead: GMP Compliance, you will play an important part at U473 (FCRS = US473) Novartis Innovative Technologies Inc in NC, United States.
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