Mq Downstream Specialist

Pfizer Com Ec

Clinical and commercial drug batch review
Product and process document evaluation
Deviation identification and resolution
Your contributions have a direct impact on patient care by upholding a quality culture that adapts and evolves to meet patient needs

Job Summary

  • Your contributions have a direct impact on patient care by upholding a quality culture that adapts and evolves to meet patient needs.
  • In this role, you will evaluate and review clinical and commercial drug batches, ensure product and process documents meet specifications, and address deviations from manufacturing standards.
  • You will maintain inspection readiness, support regulatory inspections, and assist manufacturing staff in real-time compliance error detection and resolution.

Matching Summary

Your contributions have a direct impact on patient care by upholding a quality culture that adapts and evolves to meet patient needs.

Skills & Requirements

Must-have

  • clinical and commercial drug batch review
  • product and process document evaluation
  • deviation identification and resolution
  • investigation approval and change control
  • cGMP standards adherence
  • regulatory and customer inspection support

Nice-to-have

  • team effectiveness skills
  • problem solving under direction
  • real-time compliance error detection
  • Quality Risk Management assessments
  • AI tools for problem solving

Key Requirements

  • Bachelor's degree or Associate's degree with 4 years experience
  • High school diploma with 6 years experience
  • Pharmaceutical industry experience
  • Quality administered systems experience
  • Current Good Manufacturing Practices knowledge

Work Rights

Not specified

Tailored Resume

Cover Letter