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Sanofi

Quality Assurance Specialist Afternoon

Toronto, ON

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hirly's read of this role

Role family
Engineering
Seniority
Mid level
Country
CA
Work mode
On-site / unstated
First seen by hirly
29 Sept 2026

Derived automatically from the posting. Upload your resume above to see how the role scores against it.

the posting

R2871753 Quality Assurance Specialist Afternoon (Weekends)

Location: Toronto, ON

Duration: Fixed term, 12 months

afternoon shift (Fri to Tue - 4pm to 12am)

About the job

At Sanofi, we chase the miracles of science to improve people's lives. We are dedicated to making a positive impact on the lives of patients and their families by developing innovative therapies and ensuring the highest standards of quality and safety. Our team is united by a shared purpose — transforming the practice of medicine by working to turn the impossible into the possible. Join us and help shape the future of healthcare.

The Quality Assurance team serves as a critical guardian of patient safety and product excellence through rigorous GMP record review and batch release activities, while fostering a culture of quality ownership and continuous improvement across operations. Through systematic oversight and shopfloor expertise, we proactively identify and mitigate quality risks, maintain robust quality systems, and ensure full regulatory compliance. Our collaborative partnerships across all functions embed quality principles into every aspect of operations, enabling the timely delivery of high-quality products to patients while upholding the highest standards of operational excellence.

This role is for an weekend's afternoon shift (Fri to Tue - 4pm to 12am) - subject to change as per business needs.

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:

  • Ensure all activities are conducted in compliance with applicable regulatory requirements and Good Manufacturing Practices (GMP)
  • Conduct regular audits of production processes to identify and address potential quality issues
  • Collaborate closely with production teams to maintain quality standards throughout the product lifecycle, with a strong shopfloor presence
  • Manage and resolve quality-related issues in a timely and effective manner
  • Monitor and analyze quality performance metrics, implementing corrective actions as needed
  • Lead root cause analysis investigations for quality incidents and implement preventive measures
  • Participate in internal and external audits and regulatory inspections, providing support and documentation
  • Develop and implement risk management strategies to mitigate potential quality issues
  • Foster a culture of quality and continuous improvement across the organization
  • Provide QA support to designated APU or PCU units on site as required

About You

Qualifications & Experience:

Education

Bachelor's degree or higher in Pharmacy, Chemistry, Biochemistry, Life Sciences, Chemical Engineering, Engineering or a related scientific field

Experience

  • 2–5+ years of experience in pharmaceutical quality assurance or operations
  • Demonstrated experience in Drug Substance/Drug Product (DP) quality operations
  • Working knowledge of cGMP and GxP regulations in a regulated pharmaceutical environment
  • Experience with quality documentation, compliance activities, and regulatory requirements
  • Familiarity with change control processes and quality systems
  • Background in process improvement and quality investigations

Key Competencies & Skills:

  • Quality Assurance and Change Control Processes
  • Inspection Readiness
  • Root Cause Analysis (RCA) and Preventive Action
  • Regulatory Requirements and QA Standards
  • Documentation Review
  • Manufacturing Processes and Product Quality Assurance
  • Risk Management
  • Cross-Team Communication and Collaboration
  • Stakeholder Management

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 a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
  • Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs.

This position is for a new vacant role that is now open for applicatio ns.

AI Usage

"Artificial Intelligence” refers to any systems that use automated processes, including algorithms and machine learning, to analyze data and make predictions, inferences, decisions, or recommendations without direct human involvement. These systems may process personal information to identify patterns, improve services, or support decision-making. The Company may use Artificial Intelligence for purposes including, but not limited to, resume screening and hiring, scheduling interviews or meetings, conducting surveys, matching skills with potential job openings, interview scoring, ensuring compliance with regulations applicable to our industry, and activities related to performance evaluation. Information collected and processed by the Company’s Artificial Intelligence systems may include the personal information detailed above and calendar availability. It excludes the information collected and processed for monitoring purposes. You should contact Human Resources if you have a question or concern regarding your personal information. You can also contact Canada’s Privacy Officer via Sanofi’s data subject request portal, Data Subject Rights Webform . The Data Subject Rights Webform can also be used to request access or correction of your personal information and file a complaint.

Sanofi is an equal opportunity employer committed to diversity and inclusion. Our goal is to attract, develop and retain highly talented employees from diverse backgrounds, allowing us to benefit from a wide variety of experiences and perspectives. We welcome and encourage applications from all qualified applicants. Accommodations for persons with disabilities required during the recruitment process are available upon request.

  • #GD-SP ​
  • #LI-SP

#LI-Onsite​

Pursue progress , discover extraordinary

Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.

At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.

Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com !

North America Applicants Only

The salary range for this position is:

76,200.00 - 110,100.00 Final compensation will be determined based on demonstrated experience, skills, location, and other relevant factors. Employees may be eligible to participate in Company employee benefits programs, and additional benefits information can be found through the (CA) LINK OR (US) LINK .

La fourchette salariale pour ce poste est la suivante:

76,200.00 - 110,100.00 La rémunération finale sera déterminée en fonction de l'expérience démontrée, des compétences, du lieu de travail et d'autres facteurs pertinents. Les employés peuvent être admissibles à participer aux programmes d'avantages sociaux de l'entreprise, et des informations supplémentaires sur les avantages sociaux peuvent être trouvées via le lien

Original posting on Sanofi's site ↗

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