Quality Compliance Associate II

Role: Quality Assurance Specialist supporting GMP compliance at Supernus Pharmaceuticals, focused on documentation review, facility inspections, and audit readiness within CNS drug development. Responsibilities: review GMP documentation, participate in internal and external audits, maintain compliance systems according to CFR/FDA guidance, and support inspection preparedness. Qualifications: B.S. in life sciences, 2+ years in GMP/GCP/GLP environments, strong understanding of regulatory standards, and proficiency in technical writing. Preferred: familiarity with pharmaceutical equipment, validation concepts, and auditing experience. High-Value: GMP compliance, documentation oversight, CFR/FDA guidance, CNS therapeutic focus, and inspection support. WorkSetup: on-site in the U.S., no travel specified.