Use Your Power for Purpose

Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our flexible, innovative, and customer-oriented culture is rooted in science and risk-based compliance. Whether you are engaged in development, maintenance, compliance, or research analysis, your contributions have a direct impact on patient care. By being part of our team, you help uphold a quality culture that adapts and evolves to meet the needs of patients, ensuring that every product we deliver is of the highest standard. Your role is crucial in maintaining this commitment and driving forward our mission to improve patient outcomes.

What You Will Achieve

As a QA Associate – Inventory Management, the successful candidate will provide quality touchpoints across the lifecycle of GMP materials—from receipt, storage, and inventory control through disposition and release—while ensuring compliance with regulatory and internal standards.

This role will also support cross-functional processes such as the Global Material Review Panel (GMRP) and collaborate closely with Pharmaceutical Sciences Small Molecule (PSSM) business lines and Operations Quality partners.

This role does not have direct reports.What You Will Achieve

• Provide QA oversight and support for GMP operations within the Global Inventory Management Group

• Support the Global Material Review Panel (GMRP) process, including review and disposition activities

• Provide QA oversight and Quality Operations GMP release support for excipients, processing aides, packaging components, and other materials

• Support handling and disposition of GMP materials aligned with inventory and manufacturing needs

• Review and approve quality records such as investigations, deviations, and commitments

• Support compliance and inspection readiness activities

• Support documentation lifecycle activities, including procedure administration and records management

• Collaborate with OQ and business partners to ensure alignment with global procedures, internal quality standards, and regulatory requirements

• Contribute to SOP development through authoring, review, and approval

• Identify opportunities and support continuous improvement initiatives

• Maintain effective cross-functional partnerships

• Ensure adherence to regulatory and internal compliance standards.

Here Is What You Need (Minimum Requirements)

• Bachelor's degree with any years of experience, or an Associate's degree with 4 years of relevant experience, or a high school diploma (or equivalent) and 6 years of relevant experience

• Experience in the pharmaceutical industry and Quality administered systems

• Sound knowledge of current Good Manufacturing Practices (part of GxP)

• Ability to work effectively in a team environment, both within one's own team and interdepartmental teams

• Effective written and oral communication skills

Bonus Points If You Have (Preferred Requirements)

• Experience at a manufacturing site.

• Managing and writing deviations

• Experience in production batch record review, Enterprise Resource Planning system, investigation of non-conformance, root cause analysis and change control management

• Strong problem-solving skills

• Ability to work independently and as part of a team

• Excellent time management and multitasking abilities

• Experience using common AI tools, including generative technologies such as ChatGPT or Microsoft Copilot, to support problem solving and enhance 

This is a 1st shift schedule position

  
Work Location Assignment: Hybrid

OTHER JOB DETAILS

Last Date to Apply for Job (Internal Candidates): July 10th, 2026

Last Date to Apply for Job (External Candidates): July 17th, 2026


The annual base salary for this position ranges from $68,600.00 to $114,300.00. 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 Pfizer Candidate Site – U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.





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 on Pfizer Careers.


Quality Assurance and Control