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) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at…