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Stark Pharma

GMP QA Compliance Lead – Biopharma (Onsite)

Stark Pharma, Indiana, Pennsylvania, us, 15705

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A biopharmaceutical company located in Indianapolis, IN is seeking a QA Compliance Specialist to ensure compliance with quality systems in a GMP-regulated environment. This role involves managing QA compliance programs, maintaining inspection readiness, and supporting regulatory activities. Ideal candidates will have over 8 years of experience in the biopharmaceutical sector along with strong knowledge of cGMP and FDA regulations. This position requires onsite collaboration with cross-functional teams. #J-18808-Ljbffr