Senior Quality Assurance Specialist

Overview

Pfizer’s unwavering commitment to quality ensures the delivery of safe and effective products to patients. In this role, you will support Pfizer’s science and risk‑based compliant quality culture by contributing to the development, maintenance, compliance, and research analysis that directly impacts patient care.

• 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 Good Manufacturing Practices (cGMP) impacts.
• Investigate and document Quality Assurance deviations, escalating issues to the Quality Assurance Lead as needed.
• Ensure regulatory compliance with current Good Manufacturing Practices (GxP) and provide Quality Review and oversight of site documentation to meet global regulatory and Pfizer quality standards.

• Bachelor’s degree with at least 2 years of experience; or a master’s degree with 0+ years; or an associate’s degree with 6 years; or a high school diploma (or equivalent) with 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 an understanding of responsible AI practices, including risk management and ethical use.

Must be able to aseptically gown. All candidates must not be allergic to penicillin. Able to lift 25–30 lbs.

Work Location Assignment:
On Premise
Last Date to Apply for Job:
July
272026
Annual base salary: $82,700.00–$
Eligible for Pfizer’s Global Performance Plan with a bonus target of 10.0% of the base salary.
Benefits: 401(k) plan with Pfizer match, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, medical, prescription drug, dental and vision coverage.
Relocation assistance may be available based on business needs and eligibility.
Not eligible for U.S. work visa sponsorship (e.g., TN, O‑1, H‑1B).

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 gender expression, national origin, disability, or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA.

Pfizer is an E‑Verify employer. This position requires permanent work authorization in the United States.

Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. This includes reporting names, addresses and the type of payments or other value received. If you are a licensed physician and Pfizer reimburses recruiting expenses, those expenses may constitute a reportable transfer of value under the federal transparency law.