Validation Engineer I

pfizer.co.ke

Base: $68,600.00 - $114,300.00; bonus/equity: 7.5%...
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Cgmp production
Cleaning validation
Equipment changeover
** Pfizer is seeking a Validation Engineer I to support the qualification of manufacturing processes and equipment in compliance with GMP standards. This hybrid role requires a degree or relevant experience and includes responsibilities such as coordinating validation activities, performing temperature mapping, and managing validation documentation. **

Job Summary

  • This role will provide validation support related to qualification of manufacturing processes and equipment used for cGMP production of phase I/II clinical drug substance supporting the Pfizer Biotherapeutics portfolio.
  • Responsibilities include coordinating and executing validation deliverables, supporting IQ/OQ/PQ activities, managing validation schedules, and reviewing and completing validation documentation.
  • We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life’s moments.

Matching Summary

Match Score: 75

** Pfizer is seeking a Validation Engineer I to support the qualification of manufacturing processes and equipment in compliance with GMP standards. This hybrid role requires a degree or relevant experience and includes responsibilities such as coordinating validation activities, performing temperature mapping, and managing validation documentation. **

Salary

Base: $68,600.00 - $114,300.00; Bonus/Equity: 7.5% of base salary; Benefits: Comprehensive benefits package including 401(k), paid time off, medical, dental, vision

Skills & Requirements

Must-have

  • cGMP production
  • cleaning validation
  • equipment changeover
  • chamber qualification
  • sterilization qualification
  • steam quality testing
  • temperature mapping
  • periodic review
  • execute against SOPs
  • document entries compliantly

Nice-to-have

  • continuous improvement mindset
  • operational excellence
  • AI tools for problem solving
  • generative technologies

Key Requirements

  • Bachelor's degree with 0+ years experience
  • Associate's degree with 4 years experience
  • High school diploma with 6 years experience
  • GMP biotechnology manufacturing experience
  • Team member in a matrix development team
  • Strong analytical and computer skills
  • Excellent oral and written communication skills
  • Maintain a safe work environment

Work Rights

Permanent work authorization

Tailored Resume

Cover Letter