Use Your Power for Purpose

Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our innovative, flexible, 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.

What You Will Achieve

In this role, you will:

• Evaluate, review, and approve validation master plans, protocols, and reports, ensuring compliance with company standards and regulatory requirements.

• Troubleshoot validation issues for equipment and performance processes, providing expertise for resolution.

• Conduct statistical analysis of testing results and process anomalies and provide high-level data analysis support for Quality Investigations.

• Guide the writing, review, and approval of validation process documents and technical reports, ensuring adherence to the latest Pfizer Quality Standards.

• Contribute to moderately complex projects, manage time effectively, and develop plans for short-term work activities.

• Manage routine Quality systems such as Change Control, Quality Agreement, Documentation, and Investigations, and coordinate testing with functional groups.

• Maintain the Site Validation Master Plan, support regulatory audits, and represent validation on site or network teams.

• Support product transfers, new product development, regulatory queries, cost improvement projects, and ensuring integration of validation schedules in production and participating in deviation investigations.

Here Is What You Need(Minimum Requirements)

• High school diploma (or equivalent) with 6+ years of experience or associate’s degree with 4+ years of experience or BA/BS with 2+ years of experience or MBA/MS with any years of relevant experience

• English intermediate level (verbal, written and listen)

• Proven expertise in Good Manufacturing Practices

• Strong working knowledge of various quality systems and processes

• Familiarity with information systems such as Global Document Management System, System Application & Products, and Quality Tracking System

• Excellent verbal and written communication skills

• Ability to work independently and in a team environment

Bonus Points If You Have(Preferred Requirements)

• Strong technical knowledge with validation/qualification of pharmaceutical processes, equipment, utilities, facilities, and/or computer systems

• Strong analytical and problem-solving skills

• Strong organizational and time management skills

• Ability to mentor and guide other colleagues

• Experience in regulatory audits and compliance

• Experience using common AI tools, 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

  Work Location Assignment: On Premise

OTHER JOB DETAILS:

Last Date to Apply for Job: March 2nd, 2026

EEO (Equal Employment Opportunity) & Employment Eligibility

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, or disability.

Quality Assurance and Control: