Group Manager - Quality Control

Qualification, Calibration & Lifecycle Management Ensure equipment qualification and lifecycle compliance for QC laboratory instruments, including IQ/OQ/PQ activities. Oversee calibration, preventive maintenance, and requalification of QC equipment in accordance with approved schedules and regulatory requirements. Ensure Equipment Qualification protocols, reports, deviations, and change controls are reviewed and approved. Collaborate with Engineering, Validation, and QA to support: New equipment introduction Decommissioning and replacement activities Qualification impact assessments for changes Ensure data integrity, ALCOA+ principles, and computerized system compliance for analytical instrumentation. Stability Management Approve and manage stability and retention sample requests, protocols, reports, and annual submissions. Ensure sponsor‑site stability samples, review of shipment temperature excursions, and execution of stability studies at site. Ensure PRQ and qualification of stability chambers as per approved schedules. Compliance, Audits & Quality Systems Ensure alignment with c GMP, regulatory requirements, and Pfizer Quality Standards across all QC activities. Represent CQ during internal, external, customer, and regulatory audits and inspections. Support timely investigation and closure of Incidents, Deviations, CAPAs, and Change Controls, including cross‑functional impact assessments. Ensure personnel safety, safe material handling, and adherence to EHS requirements within QC laboratories. Continuous Improvement & Technical Excellence Guide analysts in the application of continuous improvement tools such as standard work, visual management, LEAN, and Six Sigma methodologies. Drive simplification, digitization, and efficiency improvement initiatives across CQ processes. Provide technical expertise in troubleshooting analytical methods, instruments, and laboratory issues. Support method transfers from R&D to QC and ensure readiness for routine testing. Collaboration & Business Partnership Partner with Manufacturing, QA, Engineering, R&D, Supply Chain, and external customers to support site objectives and timelines. Establish and monitor departmental performance metrics to drive operational effectiveness. Communicate complex technical concepts clearly, solicit feedback, and influence stakeholders using sound scientific and business rationale. Here Is What You Need (Minimum Requirements) EDUCATION: B. Pharm / M. Pharm / M.Sc. Experience: Minimum 10+ years of pharmaceutical industry experience with a strong background in Quality Control. Extensive knowledge of c GMP compliance for Quality Control laboratories, including, testing, stability management, lab investigations, equipment qualification, and data integrity. Demonstrated experience in: Analytical testing, stability management, and retention samples Equipment qualification, calibration, and maintenance oversight Audit handling and regulatory inspections Incident, CAPA, Change Control management People leadership and performance management Proficiency in a wide range of analytical techniques and QC instrumentation. Bonus Points If You Have (Preferred Requirements) Master's degree Knowledge in the application of statistical tools, root cause analysis, and/or six sigma methodologies Experience with environmental testing, utility monitoring, analytical testing, microbial identification, and sterility testing Expertise in QC instrumentation, qualification, and troubleshooting Experience in setting requirements for the transfer of methodology from Research and Development (R&D) Ability to manage projects and ongoing work activities of moderate complexity Excellent verbal and written communication skills Ability to foster teamwork and colleague development Experience using common AI tools, including generative technologies such as Chat GPT or Microsoft Copilot, to support problem solving and enhance productivity. Demonstrated curiosity for exploring how these tools can improve outcomes and understanding of responsible AI practices, including risk management and ethical use Work Location Assignment: On Premise Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates. To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on Pfizer Careers. Quality Assurance and Control Pfizer careers are like no other. In our culture of individual ownership, we believe in our ability to improve future healthcare, and potential to transform millions of lives. We’re looking for new talent to join our global community, to unearth new innovative therapies that make the world a healthier place.