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
In this role, you will:
- Identify and address deviations from manufacturing and packaging standards.
- Approve investigations and oversee change control activities to maintain compliance with configuration management policies.
- Contribute to project tasks and milestones, organizing work to meet deadlines.
- Learn and apply basic team effectiveness skills within the immediate work team.
- Make decisions within limited options to resolve basic problems under supervisor's direction.
- Maintain inspection readiness, support regulatory and customer inspections, and improve quality assurance systems.
- Assist manufacturing/packaging staff in real-time compliance error detection and resolution, and lead or participate in Quality Risk Management assessments.
- Prepare and communicate monthly quality performance metrics.
Here Is What You Need (Minimum Requirements)
- Bac + 5 or Degree in Pharmacy, Biology, Chemistry, or related field.
- Experience in pharmaceutical industry / quality assurance or a similar regulated environment.
- Strong knowledge of GMP, regulatory compliance, and quality systems.
- Excellent analytical, organizational, and communication skills.
- Effective written and oral communication skills
Bonus Points If You Have (Preferred Requirements)
- Experience at a manufacturing site.
- Managing and writing deviations
- 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 Microsoft Copilot, to support problem solving
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
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