Dir, Quality Assurance Operations

Join to apply for the Dir, Quality Assurance role at Alkermes Management of Quality Assurance functions across the Wilmington, Ohio site. Ensure compliance with FDA, EU, and other regulations, and maintain inspection readiness. Interface with regulatory agencies, customers, consultants, and corporate functions. Major Responsibilities: Decision-making on quality assurance matters, policy and standard improvements (25%) Staffing, training, and personnel development (25%) Oversight of batch review, manufacturing activities, product release, and clinical release (25%) Management of quality systems including deviations, investigations, complaints, audits, data integrity, and compliance (25%) Qualifications: Team-oriented, detail-focused, organized, innovative, adaptable, capable of managing multiple tasks Strong communication skills Leadership with influence, coaching, and collaboration skills Experience in FDA-regulated pharmaceutical manufacturing Knowledge of regulatory compliance, process validation, technology transfer, and software skills Ability to analyze complex technical issues and make compliant decisions Expertise in pharmaceutical quality operations, parenteral and oral dosage experience preferred Experience in CGMP compliance for clinical to commercial products Education & Experience: Bachelor of Science degree 15+ years in pharmaceutical industry with progressive quality leadership At least 5 years in managerial quality roles Work Conditions: On-site, flexible hours, occasional travel. No special physical requirements. About Alkermes: A biopharmaceutical company dedicated to neuroscience, with a focus on psychiatric and neurological disorders. Committed to diversity, inclusion, and making a positive impact on patients’ lives. Recognized as a Great Place to Work and other awards. Seniority level: Director Employment type: Full-time Job function: Quality Assurance #J-18808-Ljbffr Alkermes