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Technical Manager, Vaccine Downstream Industrialization (new vaccine production facility)

Toronto, Canada

Sanofi, in the U.S. and Canada, strives to create a diverse and inclusive work environment that empowers employees to drive their careers and be successful. The talent we look for will contribute to the organization in innovative, insightful, and creative ways in order to strengthen our dynamic culture and drive us collectively to make a difference in the lives of patients.

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  • HEALTH AND WELLNESS PROGRAMS

    Comprehensive coverage including medical, dental, vision, and health and wellness programs.

  • EMPLOYER MATCHING

    Employer matching because Sanofi invests in their employees!

  • PROFESSIONAL DEVELOPMENT

    Sanofi is eager to further your development and expertise in an ever challenging environment.

  • FAMILY SUPPORT

    Sanofi understands the importance of family. We offer a variety of support including maternity/paternity leave.

  • PAID TIME OFF

    Enjoy 3 weeks’ vacation and paid holidays, including company shutdown at the end of every year!

  • WORK/LIFE BALANCE

    Importance of life outside of the office is valued at Sanofi.

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Responsibilities

Responsibilities

The B100 MTech Technical Manager, Vaccine Downstream Industrialization, will work with the Downstream Lead, with the following key accountabilities:

  • Secure optimized and robust industrialization of vaccine product downstream process in the new B100 bulk manufacturing facility
  • Deliver a strong and comprehensive characterization and validation package in collaboration with the MTech B100 team and other key players (ARD, AP&T, BRD, QC, etc)
  • Support the design and qualification of downstream process equipment to ensure full compliance to process specifications/ requirements, industry standards and quality aspects
  • Ensure effective and logical process adaptation in the framework of a new facility

Deliver on Design and Qualification Phases

  • Review process flow diagrams, mass balances and process descriptions and process assessments/impacts including critical parameters
  • Participate in Design Qualification for process equipment to ensure alignment with process requirements and specifications
  • Review equipment design and automation (FS, DDS, P&ID, GA drawings, etc)
  • Assess new technology implementations , including closed systems and single-use technology
  • Support C&Q activities: including (but not limited to) pre-FAT inspections, FAT, SAT, IQ, and OQ of the applicable process equipment/systems in conjunction GEM, Operations and Quality/validation

Downstream Process Development, Optimization and Validation

  • Oversee design and execution of scale-down of manufacturing processes to support validation and characterization.  
  • Demonstrate adequacy of the solutions selected with the process needs.
  • Collect and properly interpret data generated from execution of studies.
  • Perform process development and validation with industrial equipment, that includes in-line dilution systems, chromatography systems, columns, centrifuges, ultra-filtration and filtration systems
  • Execute process validation studies, developing detailed validation and study protocols/reports related to process, cleaning, decontamination, and related supportive studies.

Transversal Support

  • Assist in sample and material management during engineering, technical and consistency batches
  • Provide training  on operation/use of process equipment (within  areas of equipment specialization)
  • Ensure process knowledge transfer throughout all phases of project execution up to and including consistency lots and regulatory preparation
  • B100 MTech Technical Manager, Vaccine Downstream Industrialization will work in an office, manufacturing and lab environments including full gowning/PPE during manufacturing phase (technical and consistency batches)
  • Some travel required in North America and Europe (planned travel ~5%)

Requirements

  • Minimum BSc or BEng in Chemistry, Chemical Engineering, Biochemistry, or related field
  • Minimum 3 years direct technical experience in biotech R&D and/or quality within manufacturing, biopharma or life science industry (GMP)
  • Hands-on experience with chromatography systems, protein purification, TFF systems, centrifuges, filtration systems and single-use technology
  • Experience in process industrialization of a biopharm/pharma product
  • Min 1 year Equipment and/or process validation experience in a GMP or highly regulated environment

Sanofi Pasteur: The world’s leading vaccine company

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.

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

#GD-SP #LI-SP

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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