Associate, ESOQ Regulatory Operations

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From Pfizer’s original posting

Use Your Power for Purpose Every day, everything we do is driven by an unwavering commitment to delivering safe and effective products to patients. Our quality culture, grounded in science and risk-based compliance, is both flexible and innovative, always putting the customer first. Whether your role involves development, maintenance, compliance, or analysis through research programs, your contributions are vital and will have a direct impact on patients. Your efforts will ensure that our products meet the highest standards of quality and safety, directly impacting the well-being of patients worldwide. What You Will Achieve In this role, you will: • Support Post Approval Changes, initial registrations and/or renewals. • Perform preliminary regulatory impact assessment, facilitate discussions and raise the change management records in the relevant GMP system/s. • Coordinate the collection of supporting documents for Post Approval Changes, initial registration, renewals, Board of Health (BOH) queries, and regulatory commitments. • Act as a liaison between CMOs and internal Pfizer functions to ensure timely progression of change activities. • Act as a regulatory expert within the…