QA Manager - Investigation Review

We’re in relentless pursuit of breakthroughs that change patients’ lives. We innovate every day to make the world a healthier place.

Pfizer Global Supply proudly shoulders the responsibility of manufacturing and distributing our wide‑range pharmaceutical products. Pfizer offers competitive compensation and benefits programs designed to meet the diverse needs of our colleagues.

• Lead and guide moderately complex projects, managing time and resources effectively and applying skills and discipline knowledge to departmental work.
• Make decisions to resolve moderately complex problems, develop new options guided by policies, and operate independently in ambiguous situations.
• Utilize judgment and experience to become a resource for others and evaluate clinical and commercial drug batches to ensure adherence to specifications.
• Identify deviations in manufacturing and packaging processes, approve investigations and change control activities, and guide operational teams in project management.
• Prepare forecasts for resource requirements, identify areas for improvement, and facilitate agreements between different teams using leadership skills.
• Assess supplier operations for regulatory compliance, conduct quality reviews, and report results to relevant medical and quality groups.
• Support the development of country quality strategic initiatives, lead continuous inspection readiness, and drive effective management of quality issues and CAPAs.
• Participate in internal cGMP audits, support regulatory inspections, perform disposition of clinical trial materials, and communicate with internal and external customers to resolve project‑related issues.
• Ensure effective internal networking to develop and maintain business partner relationships with internal colleagues.

• BA/BS with at least 4 years of experience or MBA/MS with at least 2 years of experience or PhD/JD with any years of experience or associate’s degree with at least 8 years of experience or high school diploma (or equivalent) with at least 10 years of relevant experience.
• Substantial experience in pharmaceutical manufacturing and quality control.
• Familiarity with Current Good Manufacturing Practices (cGMP) and handling compliance issues arising from cGMP deviations or product defects.
• Knowledge of regulations related to vendor management programs and other industry quality systems.
• Strong critical thinking skills and a proactive approach.
• Ability to collaborate effectively, manage relationships, and communicate well both in writing and verbally.
• Advanced computer skills in MS Office applications and a good understanding of enterprise systems such as PDM, Quality Tracking System Trackwise, and Documentum platforms.

• Experience in Quality Systems in pharmaceutical, medical device, or combination product industry.
• Knowledge or exposure to data science.
• Strong leadership and team management skills.
• Ability to work under pressure and meet tight deadlines.
• Ability to influence and negotiate with stakeholders.
• Experience in conducting internal audits and supporting regulatory inspections.
• 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.

• Last day to apply:
  January 30, 2026.
• Relocation support available.
• Work location assignment: on‑premise.
• Annual base salary ranges from $99,200.00 to $. Eligible for participation in Pfizer’s Global Performance Plan with a bonus target of 12.5% of base salary and long‑term incentive program.
• Comprehensive benefits 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 (medical, prescription drug, dental and vision coverage). Learn more at Pfizer Candidate Site – U.S. Benefits (usca).
• Relocation assistance may be available based on business needs and/or eligibility.

Sunshine Act:
Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. Qualified physicians may see their name, address and the type of payments or other value received reported to the government.

EEO & Employment Eligibility:
Pfizer is committed to equal opportunity in all employment. The position requires permanent work authorization in the United States.

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