Spécialiste, Validation / Specialist, Validation
- Kirkland, QC
- On-site
- Posted Sep 18, 2026
- 1 position
Opens LinkedIn
- Employment type
- Full-time
- Experience level
- Entry, Junior · 0+ years
- Minimum education
- Bachelor’s degree
- Posting language
- English
- Working hours
- 40 hours per week
- Seniority
- Not Applicable
- Application method
- Direct apply is available
Job summary
Develop and execute qualification protocols for equipment, computerized systems, and manufacturing operations with a focus on sterilization. Provide technical support for the design, installation, and production of new and existing systems while ensuring compliance with corporate and cGMP standards.
Job details
Develop and execute qualification protocols for equipment, computerized systems, and manufacturing operations with a focus on sterilization. Provide technical support for the design, installation, and production of new and existing systems while ensuring compliance with corporate and cGMP standards. Requires a Bachelor's degree in Engineering or Science and at least one year of experience in pharmaceutical manufacturing. Candidates must have hands-on experience writing qualification documents and be proficient in both English and French.
What you’ll do
Develop and execute qualification protocols for equipment, computerized systems, and manufacturing operations with a focus on sterilization. Provide technical support for the design, installation, and production of new and existing systems while ensuring compliance with corporate and cGMP standards.
Requirements
Requires a Bachelor's degree in Engineering or Science and at least one year of experience in pharmaceutical manufacturing. Candidates must have hands-on experience writing qualification documents and be proficient in both English and French.
Benefits
- Health Insurance
- Dental Insurance
- Disability Insurance
- Group Retirement Plan
- Wellness Programs
Listed skills
- Microsoft Office · Preferred
- Project management · Preferred
Other relevant skills
Identified from the job description. Confirm important requirements above.
- Validation Protocol Development
- Sterilization Validation
- cGMP Regulations
- Equipment Qualification
- Change Control
- Microsoft Office
- Bilingual Communication (French and English)
- Analytical Problem Solving
- Technical Writing
- Project Management
Job areas
- Manufacturing
- Engineering
- Science & Research
- Healthcare
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