Sanofi Group MES User Project Lead in Toronto, Ontario

MES (Manufacturing Executing System) User Project Lead

Location: Sanofi Pasteur – Toronto, Canada

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.

Mission

In the scope of the new building B100 in Toronto for vaccines production, the Core Model MES Inova (Pas-X of Werum) will be deployed and calibrated to the site requirements. The UPL will be in charge of this implementation for the business. This position also provides project management for the deployment of the MES. The position is a professional position and reports to the IMS Operation Leader.

Key accountabilities

  • Collaborate to define project scope, goals and deliverables that support business objectives in collaboration with all stakeholders

  • Will coordinate the project execution and directs projects phases from inception through completion, including “go-live”. Plans, designs, develops and systems and solution.

  • She/he proactively proposes adaptations to the project plan to overcome difficulties or requirements change (will manage the MES risk matrix).

  • She/he is responsible for complying with the committed project budget, timelines and quality requirements.

  • She/he will facilitate scheduled meetings, document defined purpose and individuals involved through use of a communications plan.

  • The UPL will also communicate on the project’s progression, will manage issues and crises, and is responsible for proactively proposing adaptations to the project plan.

  • Establishes design concepts, criteria and engineering efforts for the project. Establishes milestones and monitors adherence to master plans and schedules identifies project problems and obtains solutions, such as allocation of resources or changing contractual specifications.

  • Directs the work of contractors assigned to the project from technical, manufacturing and administrative areas.

  • Help and Support the site towards a trajectory of digitization of its production workshops.

  • Participates in organizing training, ensuring acceptance and deployment of the solution from a user perspective.

  • He can represent the MES Business System Owner during the project.

  • Support the "Build" phase

  • Collect the required data for MES record creation (equipment, holding time associated, critical parameters….)

  • Creating and building the required electronic batch records in MES

  • Support the "UAT" phase: principle of validation of the systems in coordination with Quality, writing of the users acceptance test cases, execution of the UAT

  • Coordinate and support end-user training

Education and experience

  • Minimum University degree: Bachelor degree in computer sciences or related field.

  • Experience in processes, process design, operations and 5S in bio/pharmaceutical facilities, minimum 5 years

  • Preference for Project Management certification

  • Experience in IT infrastructure, system deployment, and maintenance (Particularly; MES, ERP, PCS, and Data analytic, minimum 7 years

  • Sound knowledge of CFR 21 part 11 and Data Integrity Risk Management.

  • Demonstrated understanding of current Good Manufacturing Practices, Health and Safety, high quality standards, industry standards and their application to the manufacturing process, minimum 5 years

  • Ability to work in a customer / client relation.

  • Must have effective problem resolution skills

Sanofi is an equal opportunity employer committed to diversity and inclusion. Our goal is to a ttract, 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.

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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, Empowering Life

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, Empowering Life