Jobs / Canada / Sanofi US Services INC
Reliability and Process Engineering Specialist
Sanofi US Services INC · 🇨🇦 Toronto, ON
Sponsorship verdict
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No government record and no wording either way. Not a refusal — ask the recruiter.
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- 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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Sponsor Radar — Sanofi US Services INC
No government sponsor record covers this employer in this country.
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About the role
R2869291 Reliability and Process Engineering 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. The Engineering and Maintenance (E&M) Reliability and Methods Department operates within the Reliability and Support Department of the broader Engineering and Maintenance organization. The Reliability and Methods Department is responsible for: • Equipment Reliability – Ensuring manufacturing equipment operates at peak performance and availability • Process Engineering – Optimizing production processes for efficiency and consistency • Preventive Maintenance – Implementing strategies to minimize downtime and extend equipment life • Spare Parts Management – Managing inventory and MRO (Maintenance, Repair, Operations) resources • Methods Development – Establishing best practices and standardized approaches to reliability engineering. 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: • Overall plant reliability (equipment, utilities, and facilities) • Monitoring of M&R value, performance, and cost effectiveness • Maintenance strategy and continuous optimization • Reliability technology (PdM, data analytics, digital WO) • Spare parts inventory optimization (criticality, stocking, FE) Additional Responsibilities: • Perform Parts Inventory Optimization (Criticality/Stocking) • Create and Optimize Preventative maintenance Tasks Lists. • Assess risks related to missed PMs and support exception management. • Review and approve Engineering/Vendor Turnover packages. • Monitor and improve M&R value through KPIs and RCM tools (FMEA, RCA, SPC). • Drive continuous improvement and failure elimination initiatives across E&M platforms. • Maintain and execute long-term asset plans, manage equipment registration, and support CAPA development. • Ensure technical governance and audit readiness, including regulatory inspection support and GMP compliance. • Participate in risk assessments, deviation review boards, and GMP documentation updates. • Perform investigations for deviations and maintenance issues, ensuring timely, thorough root cause analysis and reporting • Apply RCM tools (RCA, FMEA, SPC) and collaborate with cross-functional teams to implement preventative actions. • Participate in CAPA planning and DRB meetings for timely investigation closures. • Collaborate with Manufacturing, Quality Operations, and SMEs to ensure investigation timelines are met. • Support cross-functional teams in GMP documentation About You • Bachelor's degree in engineering with 5 years of relevant experience in manufacturing, maintenance, or engineering environments. • At least 1 year working with internal and contracted maintenance personnel in pharma or related industry. • Experience in regulatory inspections and GMP environments. • Strong investigation and problem-solving skills. • Excellent communication, organization, and technical writing abilities. • Six Sigma or equivalent root cause analysis training is preferred. • Familiarity with CMMS systems and reliability tools (RCM, FMEA, RCA, SPC). • Knowledge of cGMPs and pharmaceutical/biological manufacturing standards. • In-depth knowledge of predictive technologies is preferred. Why Choose Us? • Bring the miracles of science to