Manager Validation

We are seeking an experienced Validation Manager to lead validation activities within our pharmaceutical manufacturing operations. The successful candidate will ensure compliance with GMP and regulatory requirements while overseeing equipment qualification, process validation, cleaning validation, and related activities.

Key Responsibilities

• Lead and manage validation projects, activities, and personnel.
• Oversee equipment qualification (IQ/OQ/PQ), process validation, and cleaning validation.
• Develop and approve validation protocols, reports, and SOPs.
• Ensure compliance with GMP, Health Canada, FDA, and applicable regulations.
• Collaborate with Production, Engineering, Quality Assurance, and Technical Services.
• Support audits, investigations, CAPAs, change controls, and continuous improvement initiatives.

Qualifications

• Bachelor's degree in Engineering, Science, or a related discipline.
• 7–10 years of pharmaceutical manufacturing experience, with strong validation expertise.
• Previous management or team leadership experience.
• Strong knowledge of GMP, equipment qualification, process validation, and cleaning validation.
• Excellent communication, organizational, and problem-solving skills.
• Bilingualism in French and English is an asset.

Work Location: In person