Senior QA Specialist: Biopharma Validation & Batch Release
Listed on 2026-10-08
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Quality Assurance - QA/QC
Regulatory Compliance Specialist, QA Specialist - Analyst/Manager -
Pharmaceutical
Regulatory Compliance Specialist
Novo Nordisk in Clayton, NC seeks a Quality Assurance specialist overseeing production validation and batch release at our API manufacturing facility. You will ensure regulatory compliance and review batch documentation, deviations, change controls, and SOPs, while supporting validation projects and quality issue resolution.
Requirements include a Bachelor's in Life Sciences, Engineering, or related field, at least 5 years in pharmaceutical manufacturing, and strong knowledge of cGMP,
For the Senior QA Specialist:
Biopharma Validation & Batch Release position at Scorpion Therapeutics, we are reviewing applications now.
All applications are reviewed carefully by our team.
The position is based in Clayton, NC, United States.
This opportunity is part of our work in Bio & Pharmacology & Health, Management & Operations.
The advertised compensation is 90..
We aim to respond to suitable candidates as soon as possible.
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