Use Your Power for Purpose

Every day, Pfizers unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our science and risk-based compliant quality culture is both flexible and innovative, always putting the patient first. Whether you are involved in development, maintenance, compliance, or research analysis, your contribution directly impacts patients.

What You Will Achieve

In this role, you will:

• Perform tasks associated with maintaining Good Manufacturing Practices (cGMP) compliant Quality Control and Stability laboratories.
• Follow Environment Health and Safety requirements for site and QC laboratories.
• Perform bioburden and endotoxin testing of routine in-process and drug substance product samples.
• Support product dispositions through sample review and reconciliation.
• Support lab activities with routine inventory checks and adhoc requests.
• Operate within established HR policies and basic colleague relations guidelines.
• Write Standard Operating Procedures (SOPs), technical reports, project plans, etc

Here Is What You Need (Minimum Requirements)

• BA/BS with any years of experience
• Demonstrated experience in manufacturing or quality experience in the biotech or pharmaceutical industry
• Fundamental understanding of laboratory instrumentation function and analytical method troubleshooting
• Excellent oral, written, and interpersonal communication skills
• Knowledge of Microsoft Office applications, specifically Word and Excel
• Ability to perform complex mathematical problems and data analysis

Bonus Points If You Have (Preferred Requirements)

• A deep understanding of Microbiology testing and experience in defending laboratory practices during regulatory audits
• Proficiency in both viable and non-viable environmental monitoring within pharmaceutical manufacturing
• Solid grasp of aseptic techniques
• Strong problem-solving skills
• Ability to work independently and as part of a team
• Ability to manage multiple tasks simultaneously
• 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, includingrisk management and ethical use

NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS

Primary working shift is first shift Sunday through Thursday. Occasional holiday or other off-hours coverage may be required but will be communicated well in advance of time that is required.

PHYSICAL/MENTAL REQUIREMENTS

Ability to perform laboratory and office work which includes walking, standing, and sitting throughout a shift. Candidate must have the ability to read, comprehend and follow procedures, and effectively manipulate laboratory testing apparatus.

OTHER JOB DETAILS

Last Date to Apply for Job: Oct 28. 2026

Referral Bonus Eligibility: YES

Eligible for Relocation Package: NO

Work Location Assignment:On Premise

Relocation assistance may be available based on business needs and/or eligibility.

Candidates must be authorized to be employed in the U.S. by any employer.

U.S. work visa sponsorship (such as TN, O-1, H-1B, etc.) is not available for this role now or in the future.

To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available onPfizer Careers.