Manager, Operational Quality - Vaccines

卡湯晩; Toronto; On-site; CAD 80,000 - 120,000; Full time

Job summary

A leading global healthcare company is seeking a Manager for Operational Quality in Vaccines. This role involves ensuring compliance with quality systems and Good Manufacturing Practices while managing day-to-day operations. The ideal candidate will have a Master's degree in a relevant field and several years of experience in quality operations within the pharmaceutical industry. Join a supportive team dedicated to delivering innovative healthcare solutions and making a real impact on patients' lives.

Benefits

Comprehensive rewards package

Health and wellbeing programs

At least 14 weeks of gender-neutral parental leave

Qualifications

• 3+ years of relevant experience in Quality Operations within a Pharmaceutical or Biologics Manufacturing facility.
• 5+ years of relevant experience in Quality Operations in similar facilities.

Responsibilities

• Support Operational Quality Deputy Directors in reviewing and approving quality documents.
• Coordinate and assess Change Control Requests and CAPAs.
• Perform audits to ensure compliance with cGMP standards.

Skills

Transversal Cooperation

Strategic Thinking

Acting for Change

Striving for Results

Education

Master of Science in Microbiology, Biochemistry, or Immunology

Bachelor of Science in Microbiology, Biochemistry, Immunology, or Pharmacology

Job description

Position Title : Manager, Operational Quality - Vaccines (Open)

Posting Date : Thursday, August 22, 2024

Closing Date : Monday, September 30, 2024

We deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families. As an Operation Quality Manager within our Quality team, your role is to provide compliance support to Deputy Directors for licensed products, managing day-to-day operations in accordance with Sanofi Pasteur quality systems requirements and Good Manufacturing Practices.

We are an innovative global healthcare company helping the world stay ahead of infectious diseases by delivering more than 500 million vaccine doses annually. Across various countries, our talented teams are exploring new technologies to protect people and promote healthy communities. We chase the miracles of science every day, pursuing progress to make a real impact on millions of patients worldwide.

Main responsibilities :

• Support the Operational Quality Deputy Directors in reviewing, following up on, closing, and approving documents such as master batch records, operational log books, SOPs, SWIs, deviations, protocols, reports, and work orders within scope or delegated authority.
• Participate in project teams.
• Coordinate, investigate, and assess Change Control Requests (CCRs) and CAPAs as the designated QO Representative, determining if changes impact product and processes.
• Perform audits in conjunction with the QO Quality System Internal Auditor and Vendor Auditor, supporting GMP activities to ensure compliance with cGMP standards, site, and corporate policies.

About you

• Master of Science in Microbiology, Biochemistry, or Immunology with 3+ years of relevant experience in Quality Operations within a Pharmaceutical or Biologics Manufacturing facility.
• Demonstrate qualities such as Acting for Change, Transversal Cooperation, Striving for Results, and Strategic Thinking.
• Bachelor of Science in Microbiology, Biochemistry, Immunology, or Pharmacology with 5+ years of relevant experience in Quality Operations in similar facilities.

Why Choose Us :

• Bring the miracles of science to life alongside a supportive, future-focused team.
• Discover opportunities to grow your talent and advance your career, through promotions or lateral moves, locally or internationally.
• Enjoy a comprehensive rewards package recognizing your contributions and impact.
• Benefit from health and wellbeing programs, including high-quality healthcare, prevention, wellness initiatives, and at least 14 weeks of gender-neutral parental leave.

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Pursue, Discover

Better exists—better medications, outcomes, and science. Progress relies on people from diverse backgrounds, locations, and roles, united by the desire to make miracles happen. Let’s be those people.

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

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