Jobs / Canada / Sanofi US Services INC
QA Operations Manager, PCU Lead
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.
Canada: Express Entry no longer awards ranking points for job offers (since 25 Mar 2025); a job offer still counts toward Federal Skilled Worker eligibility.
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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.
Past sponsorship or register membership never guarantees sponsorship for this vacancy or for you. Full Sponsor Radar for Sanofi US Services INC →
About the role
Reference Number: R2872450 Position title: QA Operations Manager, PCU Lead 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. 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: 1. Quality Assurance Management: • Develop and implement annual quality assurance objectives for E&M/Distribution manufacturing, aligning with organizational strategy and vision. • Ensure compliance with GMP, regulatory requirements, and company quality standards for all E&M/Distribution production activities. • Maintain a system to identify, track, and mitigate quality risks in E&M/Distribution manufacturing. • Oversee batch release processes, including release of batches for further manufacturing and ensuring timely and compliant final disposition of completed batches. • Lead investigations into quality issues, deviations, and out-of-specification results related to E&M/Distribution. • Support other duties as required. 2. Process-Centric Unit Management: • Collaborate closely with production teams to maintain quality standards throughout the E&M/Distribution ecosystem. • Conduct regular audits of E&M/Distribution processes to identify and address potential quality issues. • Oversee all investigations related to E&M/Distribution production to ensure proper risk assessment and product impact evaluation. • Manage and resolve quality-related issues in E&M/Distribution in a timely and effective manner. 3. Quality Systems and Continuous Improvement: • Establish and monitor key performance indicators (KPIs) for E&M/Distribution quality assurance activities. • Identify and drive continuous improvement initiatives to enhance quality and operational efficiency in E&M/Distribution production. • Promote a culture of quality throughout the E&M/Distribution organization. • Evaluate and recommend new technologies, tools, and methods to enhance E&M/Distribution quality assurance processes. 4. Team Leadership and Development: • Lead and manage the E&M/Distribution quality assurance team, including hiring, training, coaching, and performance evaluation. • Ensure the team is properly qualified and trained on current GMP requirements and quality standards. 5. Regulatory Compliance and Inspections: • Participate in regulatory inspections and audits, providing expertise on E&M/Distribution quality assurance. • Ensure the site maintains valid manufacturing licenses and product permissions for E&M/Distribution. About You Education and Experience: • Minimum Bachelor's degree in Chemistry, Biochemistry, Pharmaceutical Sciences, Engineering, or related field; advanced degree preferred. • Minimum of 8 years of experience in quality roles; pharmaceutical industry preferred • Preferred experience/ in-depth knowledge of GMP regulations and guidelines. • Prefer candidate with previous management experience Skills & Qualifications: • Strong understanding of pharmaceutical manufacturing processes and associated quality control methods. • Excellent analytical and problem-solving skills, with the ability to make data-driven decisions. • Proven leadership experience in leading and coaching teams, fostering growth and innovation. • Effective communicator with strong interpersonal skills. • Interacts ef