Oversee Quality Assurance for on-market products from commercialization through end of life, ensuring compliance with all relevant standards and regulations. Maintain Good Documentation Practices (GDP), including product specifications, formula approvals, and audit documentation. Manage Third-Party Testing, coordinating all ongoing testing activities, ensuring appropriate record retention of results, Certificates of Analysis, and other relevant documentation.

Responsible for quality of assigned products which may include small molecule pharmaceuticals and/or biologics products, combination products, and medical devices to ensure business objectives are met with regards to on time delivery of product while assuring compliance to local, divisional, and corporate policies and external agency regulations worldwide. Acts as the primary quality representative for the global supply chain.