Pfizer
Pearl River, NY, USA
Use Your Power for Purpose Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our flexible, innovative, and customer-oriented culture is rooted in science and risk-based compliance. Whether you are involved in development, maintenance, compliance, or analysis through research programs, your contribution directly impacts patients. What You Will Achieve In this role, you will: Provide QA support to Manufacturing and Laboratories Focus on Quality Systems including site Change Management Accountable for the overall management of the site Change Management process; acts as gate-keeper of the change by authorizing/approving the change from plan approval through implementation and closure Assess all changes for Regulatory impact by reviewing dossier content and collaborating with GCMC Regulatory Strategists as needed Initiate PCFs in PDM for regulatory impacted changes Author/approve Annual...