Jobs / Canada / Sanofi US Services INC
Quality Control Maintenance and Qualification Specialist
Sanofi US Services INC · 🇨🇦 Toronto, ON
Sponsorship verdict
No sponsorship evidence yet
No government record and no wording either way. Not a refusal — ask the recruiter.
- No government sponsor record hereNo government sponsor record covers this employer in this country.
- The posting doesn’t mention sponsorshipSilence isn’t a refusal — ask the recruiter before investing much time.
- No salary bar for this routeCanada has no single salary bar: the employer usually needs a positive LMIA. Pay at or above the provincial median wage + 20% (e.g. C$36.92/h in Ontario) puts it in the high-wage stream. Source: https://www.canada.ca/en/employment-social-development/services/foreign-workers/median-wage.html, rules effective 2026-07-17.
- Confirmed live todayWhen a source last listed this job as open.
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Why not apply?
No register record and no sponsorship wording in the posting. Worth asking the employer before investing significant time.
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Sponsor Radar — Sanofi US Services INC
No government sponsor record covers this employer in this country.
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About the role
R2872437 Quality Control Maintenance and Qualification Specialist Location: Toronto, ON About the job Join a global network that powers how Sanofi delivers — seamlessly, purposefully, and at scale. In Manufacturing & Supply, you’ll help reimagine how life-changing treatments reach people everywhere, faster. Our Team / Overview: The Quality Control Team is part of Site Quality Operations supporting the Manufacturing & Supply organization in Toronto. The Quality Control team oversees analytical testing, product release, method validation, stability programs, and laboratory operations in alignment with regulatory requirements and Sanofi standards. The team drives continuous improvement and operational excellence initiatives to enhance laboratory efficiency, analytical capabilities, and quality systems performance. About Sanofi We’re an R&D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people’s lives. Main Responsibilities: • Executing the maintenance and qualification protocols in their area • Writing or reviewing the maintenance and qualification documentation, when not executing; this includes protocols, reports, risk assessments, and traceability matrices according to predefined timelines • Informing their manager of any quality or HSE event related to lab equipment in a timely manner to ensure investigation and impact assessment are performed appropriately • Ensuring proper documentation of deviations, non-conformances, and corrective actions • Ensuring proper evaluation (validation expertise) of change controls related to his/her scope • Ensuring all maintenance and qualification activities comply with regulatory requirements (e.g., FDA, EMA) and company quality standards • Cooperating with cross-functional teams, including engineering and external suppliers, to ensure smooth execution of validation activities • Identifying opportunities for improving maintenance and qualification processes and contributing to continuous improvement initiatives • Performing routine and preventive maintenance and qualification on equipment and systems to ensure optimal performance and reliability • Troubleshooting and repairing equipment and systems as needed to minimize downtime and ensure continuous operation • Maintaining accurate records of maintenance and qualification activities, including work orders, maintenance logs, and calibration records Key Involvement in Decision-Making Process • Execute or coordinate the maintenance and qualification plans for the lab equipment • Responsible for performing routine and preventive maintenance and qualification on equipment and systems About you • A Bachelor of Science, Engineering, or related field • 1 year of experience in qualification activities within the pharmaceutical or biotechnology industry • 1 year of experience in quality control • Proficiency in preparing maintenance and qualification documentation • Strong understanding of regulatory requirements and guidelines (e.g., FDA, EMA) related to qualification • Ability to manage multiple qualification projects simultaneously, ensuring they are completed on time and within budget • Excellent communication skills to effectively collaborate with cross-functional teams. Why Choose Us? • Bring the miracles of science to life alongside a supportive, future-focused team. • Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally. • Enjoy