Associate Manager - Quality Assurance

At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Manager, Quality Assurance to join our Quality organisation, supporting the importation and distribution of biologic products for the Canadian market in a hybrid work mode. In this role, you will provide GMP quality oversight and act as Deputy Responsible Person while collaborating with local and global Quality teams, third-party providers, and Health Canada inspectors.

This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.

Toronto, Canada (hybrid)

• Act as Deputy Responsible Person for batch compilation, review, disposition, and release of Canadian-market products.
• Provide quality oversight for timely batch disposition of commercial and clinical biologic products.
• Create, revise, and approve quality documentation, including Change Controls, Deviations, CAPAs, Complaints, SOPs, and APQRs.
• Monitor quality system metrics and act as escalation point for complex compliance issues.
• Oversee Canadian importation and distribution activities, including third-party logistics (3PL) providers.
• Serve as quality subject matter expert (SME) supporting Health Canada inspections, audits, self-inspections, and recalls.
• Collaborate with local and global Quality teams and drive continuous improvement of quality standards.
• You apply sound, risk-based judgment to resolve complex quality and compliance issues.

• Canadian Bachelor's degree in a Life Sciences field (Biology, Chemistry, Pharmacy, or equivalent) required.
• Minimum 5 years of Quality Assurance experience in pharmaceutical, biotechnology, or biologics.
• Demonstrated experience within GMP-regulated environments.
• Experience with batch record review, batch release, deviations, change controls, CAPAs, and quality systems management.
• Strong understanding of Health Canada GMP and GDP requirements, with experience supporting regulatory inspections and audits.
• Ability to work independently while collaborating across cross-functional and global teams, with excellent written, verbal, organisational, and problem-solving skills.
• Experience overseeing biologics importation and distribution in Canada, or oversight of third-party manufacturers and 3PL providers, preferred.
• Experience with medical device importation in Canada or working in a global quality organisation, an asset.

We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law.

Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.

Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive…