Responsable De La Validation - Validation Lead

Haleon

Montréal, Canada
Base: competitive salary; bonus/equity: annual bon...
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Validation lifecycle management
Site validation strategy
Equipment and facility qualification
** Haleon is seeking a Validation Lead for their Montreal facility, responsible for ensuring compliance and effectiveness of validation processes in a regulated manufacturing environment. The ideal candidate will have extensive experience in validation within the pharmaceutical or manufacturing industry and be fluent in French. **

Job Summary

  • The Validation Lead will be responsible for the supervision, management, and delivery of all elements of the validation lifecycle, defining and maintaining the site's validation strategy.
  • Key responsibilities include ensuring compliance with evolving expectations for equipment and facility qualification, process/packaging validation, cleaning validation, CPV, analytical method validation, and computerized system validation.
  • Haleon offers a competitive salary plus annual bonus, collective insurance from day one, 26 weeks of paid parental leave, 3 weeks vacation plus personal days, and a permanent full-time position with career growth opportunities.

Matching Summary

Match Score: 75

** Haleon is seeking a Validation Lead for their Montreal facility, responsible for ensuring compliance and effectiveness of validation processes in a regulated manufacturing environment. The ideal candidate will have extensive experience in validation within the pharmaceutical or manufacturing industry and be fluent in French. **

Salary

Base: Competitive salary; Bonus/Equity: Annual bonus; Benefits: Collective insurance, 26 weeks paid parental leave, 3 weeks vacation + 5 personal days, December week off, retirement plan, savings plan

Skills & Requirements

Must-have

  • Validation lifecycle management
  • Site validation strategy
  • Equipment and facility qualification
  • Process/packaging validation
  • Cleaning validation
  • Continuous Process Verification (CPV)
  • Analytical method validation
  • Computerized system validation
  • Regulatory audit compliance

Nice-to-have

  • Agile and performance-driven culture
  • Human-centered approach
  • Detail-oriented mindset
  • Innovation and excellence
  • Employee well-being focus

Key Requirements

  • Minimum 7 years of demonstrated experience in validation, automation, quality, and compliance
  • Bachelor's degree in engineering, industrial pharmacy, chemistry, or relevant scientific/pharmaceutical discipline
  • Proficiency in French required
  • Legally authorized to work in Canada

Work Rights

Legally authorized to work in Canada

Tailored Resume

Cover Letter