Pfizer
Pharmaceutical
QualityProductassociate
Neural analysis suggests this role is
optimal for Mid+ candidates.
“Quality Product associate at Pfizer. Skills: Quality assurance, Regulatory compliance, Process management. Identify and address deviations from manufacturing and packaging. Approve investigations”
What You'll Achieve.
Deliver safe and effective products; Uphold a quality culture; Improve patient outcomes
Industry & Context.
Resolve basic problems
What They're Looking For.
Must Have
Bac + 5 or Degree in Pharmacy, Biology, Chemistry, or related field, Experience in pharmaceutical industry / quality assurance or a similar regulated environment, knowledge of GMP, regulatory compliance, and quality systems, Excellent analytical, organizational, and communication skills, Effective written and oral communication skills
Nice to Have
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
What You'll Do.
Identify and address deviations from manufacturing and packaging
Approve investigations
Oversee change control activities
Contribute to project tasks and milestones
Organize work to meet deadlines
Learn and apply basic team effectiveness skills
Make decisions within limited options to resolve basic
Maintain inspection readiness
Support regulatory and customer inspections
Improve quality assurance systems
Assist manufacturing/packaging staff in real-time compliance error detection
Lead or participate in Quality Risk Management assessments
Prepare monthly quality performance metrics
Communicate monthly quality performance metrics
How You'll Work.
Team & Collaboration
Immediate work team
Communication Scope
Written communication; Oral communication
Process & Methodology
Project tasks, Milestones
Full Job Description
**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)** * E
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