Validation Engineer I

pfizer.ca

Base: $68,600.00 - $114,300.00; bonus/equity: 7.5%...
Hybrid
Cgmp production support
Qualification of manufacturing processes
Equipment changeover validation
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

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

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.

Salary

Base: $68,600.00 - $114,300.00; Bonus/Equity: 7.5% bonus target; Benefits: Comprehensive benefits package

Skills & Requirements

Must-have

  • cGMP production support
  • qualification of manufacturing processes
  • equipment changeover validation
  • cleaning validation support
  • temperature mapping
  • steam quality testing

Nice-to-have

  • continuous improvement mindset
  • operational excellence
  • AI tools for productivity

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
  • Work authorization in the United States

Work Rights

Permanent work authorization in the United States

Tailored Resume

Cover Letter