Senior Quality Assurance Specialist

Use Your Power for Purpose

Every day, Pfizer’s 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.

In this role, you will:

• Evaluate and review clinical and commercial drug batches to ensure compliance with established specifications.
• Conduct rigorous sampling and statistical process control procedures to identify deviations from standards.
• Approve investigations and change control activities to maintain compliance with configuration management policies.
• Contribute to moderately complex projects, managing time effectively and developing short‑term work plans.
• Independently assess change control activities for potential quality and operational cGMP impacts.
• Investigate and document quality assurance deviations, escalating issues to the quality assurance lead as needed.
• Ensure regulatory compliance with current GxP and provide quality review and oversight of site documentation to meet global regulatory and Pfizer quality standards.

• Applicant must have a bachelor’s degree with at least 2 years of experience; OR a master’s degree with 0+ years of experience; OR an associate’s degree with 6 years of experience; OR a high school diploma (or equivalent) and 8 years of relevant experience.
• Solid understanding of current Good Manufacturing Practices and relevant GxP regulations and standards.
• Strong critical thinking skills.
• Ability to work effectively within own team and interdepartmental teams.
• Good working knowledge of Microsoft Excel and Word.
• Proactive approach to problem‑solving.

• Experience in quality‑administered systems.
• Strong organizational skills and attention to detail.
• Experience with regulatory compliance and documentation.
• Ability to mentor and review the work of other colleagues.
• 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.

• Must be able to aseptically gown.
• This is a penicillin manufacturing facility. All candidates applying must not be allergic to penicillin.
• Able to lift 25–30 lbs.

Weeknight and weekend work may be required.

Work Location Assignment:
On Premise. Last Date to Apply for Job:
July 27, 2026.

The annual base salary for this position ranges from $82,700.00 to $. This position is eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 10.0% of the base salary. Benefits include a 401(k) plan with Pfizer matching contributions, an additional Pfizer retirement savings contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits covering medical, prescription drug, dental and vision.

Relocation assistance may be available based on business needs and/or eligibility. Candidates must be authorized for employment in the United States. U.S. work‑visa sponsorship is not available for this role now or in the future.

Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. If you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government.

Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or…