Novo Nordisk’s Bloomington, Indiana facility is seeking a Manager, QA to ensure FDA and other regulatory compliance, maintain quality systems, and lead QA operations. The role encompasses audits, documentation control, training, and cross-functional collaboration to deliver high-quality drug products.
The position requires a Bachelor’s in a related field (or equivalent with experience) and several years in cGMP/QA environments, with 1–3 years of management experience.
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This position is listed as full time and onsite.