DSRD Global Pathology Quality Control Scientist

Use Your Power for Purpose Pfizer’s purpose is to deliver breakthroughs that change patients’ lives. At the core of this mission is Research and Development, where we strive to transform advanced science and technologies into the most impactful therapies and vaccines. Whether you are involved in discovery sciences, ensuring drug safety and efficacy, or supporting clinical trials, you will leverage cutting-edge design and process development capabilities to accelerate and deliver top-tier medicines to patients globally. Through their expert knowledge in anatomic and/or clinical pathology techniques and processes, the Global Pathology Quality Control Scientist will primarily and independently conduct all aspects of Quality Control of anatomic and/or clinical pathology data, specimens and reports. Based on their qualification, they may also flex to independently perform all aspects of rodent and non-rodent routine necropsy and/or histology procedures to support investigative, exploratory, and regulatory studies of high complexity. They will independently support, develop, trouble-shoot and validate new procedures and technologies of high complexity in the field of anatomic and/or clinical pathology. What You Will Achieve In this role, you will: • Perform all regulatory responsibilities in compliance with applicable regulatory standards including Good Laboratory Practices and animal welfare regulations. • Perform Quality Control of anatomic and/or clinical pathology data, specimens and reports independently • Adheres to all study report timelines • Based on their qualifications, may flex to support necropsy, histology of exploratory, regulatory and investigative studies • Contribute to laboratory procedures and Controlled Documents • Contribute to DSRD publication data integrity Quality Control • Interact with and train individuals • Contribute to pathology scheduling tasks • Independently develop, refine, document methods/processes/reporting for assays of high complexity in the field of anatomic and/or clinical pathology (e.g. new sampling methods, non-standard endpoints) based on their scientific knowledge Here Is What You Need (Minimum Requirements) • Bachelor’s Degree biology or a related field with at least 6 years of experience or a Master’s Degree with at least 4 years of experience • ≥ 3 years in GLP environment • ≥ 2 years relevant experience in quality control • Exceptional communication skills • Strong organizational change management abilities • Proficiency in Word, TEAMS, spreadsheets, PowerPoint, and relevant scientific software Bonus Points If You Have (Preferred Requirements) • HT (ASCP) certification • Master’s degree (MS) with over 4 years of relevant experience • Strong understanding and adherence to regulatory guidelines • Proficiency in VBA, .NET, SAS, SQL Server, Oracle, and MS Access • Scripting capabilities • Experience in a research laboratory setting • Experience using common AI tools, including generative technologies such as ChatGPT 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 PHYSICAL/MENTAL REQUIREMENTS sitting, standing, walking, ability to lift 20 lbs. Work Location Assignment: On Premise     The annual base salary for this position ranges from $79,400.00 to $132,400.00. In addition, this position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 7.5% of the base salary. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments. Benefits offered include a 401(k) pla