Senior Quality Associate

Role: Quality Assurance specialist overseeing pharmaceutical manufacturing compliance and batch release. Responsibilities: verify batch conformance with GMP (21 CFR 210/211), review manufacturing/laboratory documentation, manage batch disposition, coordinate with Quality Control, Manufacturing, and Supply Chain, oversee quality systems like Change Control, and support audit and regulatory activities. Requirements: BS in chemistry, biochemistry, pharmacy, or related science; 5+ years in pharma/biotech quality roles; experience in drug product review and release; deep knowledge of GMPs and CFR 210/211; strong decision-making, communication, and adaptability skills. Preferred: ASQ certification. HighValue: pharmaceutical manufacturing, GMP compliance, batch release, CFR 210/211, quality systems management, experience with drug product release processes.