Job Description
**Job Summary:** Lead a team of Global Procurement Compliance professionals to ensure cGMP compliance in procurement operations, managing Approved Supplier List, deviation investigations, and regulatory inspections. The Senior Manager, Global Procurement - Supplier Quality Compliance will be responsible for leading a team of professionals that support and maintain all cGMP compliance aspects of procurement operations. **Key Responsibilities:** * Manage and facilitate the Approved Supplier List (ASL) to ensure compliance with cGMP regulations * Conduct deviation investigations and coordinate CAPA implementation for high-risk events * Monitor and report Key Performance Indicators (KPIs) for compliance functions, including right-first-time (RFT) for deviation investigations * Perform supplier audits and ensure successful closures by focusing on proactive issue resolutions and communication with suppliers * Lead the coordination and support of Procurement and Quality auditing needs for acceptable closure of Internal Regeneron and Supplier audit findings * Develop and maintain Procurement cGMP procedures, documentation, and training related to SOPs and Work Instructions * Continually reassess Global Procurement systems and processes for adherence to cGMPs and industry standard methodologies and implement changes/improvements as needed * Support the start-up/integration of Global Procurement compliance functions at other IOPS sites, including travel as needed * Oversee/direct the maintenance of the Approved Supplier List (ASL) and associated Periodic Review of suppliers * Lead the Supplier Review Board meeting and ensure all actions / decisions are documented and tracked appropriately **Requirements:** * Bachelor's degree plus 5-7 years of relevant, progressive experience in procurement, quality or compliance, including experience in Pharma/Bio Pharma / cGMP working environment * Managerial/supervisory experience leading collaborative teams in a global, matrixed organization * Good working knowledge of and experience in setting up and maintaining a QMS which meets the legislative requirements of human medicines in the EU and USA * Ability to leverage standard business applications for communicating, presenting and analyzing (Word, Excel, Power Point) **Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations.**