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, focusing on ensuring compliance and performance of manufacturing processes within a regulated environment. The ideal candidate will have significant experience in validation and a strong understanding of regulatory frameworks, particularly in the pharmaceutical or health product sectors. **

Job Summary

  • As a Validation Lead, you will play a strategic role at the heart of our operations, ensuring the compliance, robustness, and performance of our processes and technologies.
  • The primary mission of the Validation Lead is to ensure that process and cleaning validation, as well as implemented solutions, fully meet regulatory, technical, and operational requirements.
  • Haleon offers a competitive salary + annual bonus, collective insurance from day one, 26 weeks of paid parental leave, 3 weeks vacation + 5 personal days + one week in December, and a permanent full-time position with a great culture.

Matching Summary

Match Score: 75

** Haleon is seeking a Validation Lead for their Montreal facility, focusing on ensuring compliance and performance of manufacturing processes within a regulated environment. The ideal candidate will have significant experience in validation and a strong understanding of regulatory frameworks, particularly in the pharmaceutical or health product sectors. **

Salary

Base: Competitive salary; Bonus/Equity: Annual bonus; Benefits: Collective insurance, 26 weeks paid parental leave, 3 weeks vacation + 5 personal days + one week in December, retirement plan, savings plan, free parking & gym, on-site cafeteria

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 demonstration
  • Site Master Validation Plan (SVMP)
  • Cleaning lifecycle process

Nice-to-have

  • Agile and performance-driven culture
  • Human-centered approach
  • Detail-oriented
  • Innovation-focused environment
  • Cross-functional collaboration

Key Requirements

  • Minimum 7 years of demonstrated experience
  • Baccalaureate in engineering, industrial pharmacy, chemistry
  • French language proficiency required
  • Legally authorized to work in Canada

Work Rights

Legally authorized to work in Canada

Tailored Resume

Cover Letter