Novo Nordisk in Clayton, NC is seeking an experienced QA professional responsible for production activities and validation, ensuring compliance with health authorities and site procedures.
You will review batch reports, release API materials, handle deviations, change controls, and support quality processes on the shop floor. Strong knowledge of cGMP, validation, and quality management systems is required to succeed.
#J-18808-LjbffrSenior QA: Validation & Batch Release Specialist in clayton at Unknown Company
This position is listed as full time and onsite.