City : Toronto
Category : Manufacturing, Vaccines, Engineering and Maintenance
Industry : Pharmaceutical
Employer : Sanofi
Reference #: R2499476
Department: B100 Mtech
Location: Toronto, Ontario
About Sanofi Pasteur
Sanofi Pasteur, the vaccines division of Sanofi, is the largest company in the world devoted entirely to human vaccines. Our driving goal is to protect people from infectious diseases by creating safe and effective vaccines. Our company distributes more than 1 billion doses of vaccine each year, making it possible to vaccinate more than 500 million people across the globe. Sanofi Pasteur offers the broadest range of vaccines in the world, providing protection against 20 bacterial and viral diseases.
Sanofi is dedicated to supporting people through their health challenges. We are a global biopharmaceutical company focused on human health. We prevent illness with vaccines, provide innovative treatments to fight pain and ease suffering. We stand by the few who suffer from rare diseases and the millions with long-term chronic conditions. With more than 100,000 people in 100 countries, Sanofi is transforming scientific innovation into healthcare solutions around the globe.
The Manager, Building 100 (B100) Manufacturing Process Validation will report directly to the B100 MTech Deputy Director, Process Validation and LCM, with the following key accountabilities:
Technical Direction and Management
Manage and provide Process Validation expertise for Media and Buffer Process and cP, Dip and Tet Antigen Processes:
Support Single-Use Technology implementation and provide guidance to validation teams and users, including any outsourcing activities:
Transversal Expertise and Management:
Education and Experience:
Master or Ph.D preferred, BSc with 5+ years demonstrated leadership (project/people management).
Minimum 8-10 years direct experience in biotech pharma/biotech manufacturing, and quality environments in a process validation role.
5+ years demonstrated leadership in behavioral competencies and project/people management.
Senior technical experience and specialist expertise in process validation including cleaning validation, media and buffer validation and filter validation.
Strong understanding and direct experience with single use technology, including implementation and validation of single use systems.
Sound knowledge in biochemistry and protein chemistry is an asset.
Ability to communicate and work with a very broad spectrum of professional and technical staff to effectively manage in an efficient and practical manner.
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.
Thank you in advance for your interest.
Only those candidates selected for interviews will be contacted.
Sanofi, Empowering Life
At Sanofi diversity and inclusion is foundational to how we operate and embedded in our Core Values. We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our colleagues, patients and customers. We respect and celebrate the diversity of our people, their backgrounds and experiences and provide equal opportunity for all.
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