Novo Nordisk seeks a Site Clayton QA Finished Production representative to ensure batch release and quality oversight for validation activities. You will review complex CRs, DV/CA PA documentation, and provide coaching for audits while maintaining a validated state of equipment and processes.
The role requires strong GMP experience, regulatory knowledge, and ability to lead cross-functional investigations, with on-site Monday–Friday expectations in Clayton, NC.
#J-18808-LjbffrSenior QA Specialist – Validation & Compliance in clayton at Unknown Company
This position is listed as full time and onsite.