Senior QA Specialist: Biopharma Validation & Batch Release
Listed on 2026-10-12
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Quality Assurance - QA/QC
QA Specialist - Analyst/Manager, Production QC/QA, Regulatory Compliance Specialist -
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,
Step into the Senior QA Specialist:
Biopharma Validation & Batch Release role at Novo Nordisk in Clayton, NC, United States and grow with us.
We invite applications for the Senior QA Specialist:
Biopharma Validation & Batch Release position located in Clayton, NC, United States.
The following position is for a Senior QA Specialist:
Biopharma Validation & Batch Release with Novo Nordisk.
Our group is growing, and we are hiring a Senior QA Specialist:
Biopharma Validation & Batch Release in Clayton, NC, United States.
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