Associate - Msat (c&q)

Pfizer Com Ec

**
Validation master plans, protocols, and reports
Troubleshoot validation problems
Statistical analysis of testing results
** Pfizer is seeking an Associate for its Quality Operations team to evaluate and approve validation processes, ensuring compliance with regulatory standards. The ideal candidate will possess strong attention to detail, organizational skills, and a solid foundation in Good Manufacturing Practices (cGMP), with opportunities for growth in a collaborative environment. **

Job Summary

  • Evaluate, review, and approve validation master plans, protocols, and reports, ensuring compliance with regulatory requirements and company policies.
  • Contribute to project tasks and milestones, organizing work to meet deadlines and applying basic team effectiveness skills within the immediate Work Team.
  • Work effectively as a member of the Quality Operations (QO) cGMP training team, collaborating with Business Area Training Leads, Coordinators, and SMEs to support cGMP and site training initiatives.

Matching Summary

Match Score: 75

** Pfizer is seeking an Associate for its Quality Operations team to evaluate and approve validation processes, ensuring compliance with regulatory standards. The ideal candidate will possess strong attention to detail, organizational skills, and a solid foundation in Good Manufacturing Practices (cGMP), with opportunities for growth in a collaborative environment. **

Skills & Requirements

Must-have

  • validation master plans, protocols, and reports
  • troubleshoot validation problems
  • statistical analysis of testing results
  • Good Manufacturing Practices (cGMP)
  • regulatory requirements and company policies
  • Microsoft Office, particularly Excel

Nice-to-have

  • AI tools, including generative technologies
  • responsible AI practices
  • pharmaceutical manufacturing, packaging, QA, and QC
  • equipment qualification and calibration
  • continuous learning and professional development

Key Requirements

  • bachelor's degree with any years of experience
  • Associate's degree with 4 years of relevant experience
  • high school diploma (or equivalent) and 6 years of relevant experience
  • 2-3 years of experience in Quality assurance and / Validation function of sterile dosage form facility

Work Rights

Not specified

Tailored Resume

Cover Letter