Hybrid QA Engineer GMP Gene Therapy
Listed on 2026-09-30
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Quality Assurance - QA/QC
Regulatory Compliance Specialist
Novartis is seeking a Quality Assurance Engineer in Durham, NC, to join a GMP manufacturing environment focused on gene therapy. Hybrid work requires onsite presence at least 3 days per week, with emphasis on inspection readiness and quality improvements across engineering, validation, and operations teams.
The role requires a Bachelor’s degree in a scientific field and 5+ years in biotech/pharma, with strong GMP knowledge and experience in audits, deviations, CAPAs, and SOPs.
We are seeking a motivated Hybrid QA Engineer for GMP Gene Therapy to join U473 (FCRS = US473) Novartis Innovative Technologies Inc in NC, United States.
We would love to welcome a new Hybrid QA Engineer for GMP Gene Therapy to our team in NC, United States.
For the Hybrid QA Engineer for GMP Gene Therapy position at U473 (FCRS = US473) Novartis Innovative Technologies Inc, we are reviewing applications now.
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