Manager, Product Development Quality Assurance

Role: Quality Assurance specialist supporting clinical supply batch disposition activities within AbbVie's pipeline. Responsibilities: review and approve batch records, manage audits, ensure compliance with global GMP standards, review regulatory impacts, support product release, and lead process improvements; act as backup management support and monitor process effectiveness. Qualifications: Bachelor's in life sciences or related field; 6+ years in pharma QA, manufacturing, or testing; experience with GMP, analytical sciences, or biological/chemical processes preferred. High-Value: focus on biologics/pharmaceuticals, GxP compliance, clinical supply chain, regulatory audits, and process improvement. WorkSetup: not specified.