B100 Commissioning, Qualification and Validation (CQV) Execution – Media, Buffer, Washing & Sterilizing (MBWS) – Vaccine

Job type: Contract
Accepting BioReady™: Yes
Category: Research and Development
Education: Bachelor
Experience: 0-3 Years
Employer: Sanofi
Location: Toronto, ON
Posted: April 7, 2021
Closes: May 7, 2021

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.

Summary of Purpose:

The incumbent will coordinate/support the execution and/or execute Commissioning and Qualification protocols and test scripts of systems associated with media, buffer, washing and sterilizing areas of a strategic capital project at the Toronto site.  The project includes about 500 utility, facility and process/lab equipment systems.  This position, augmented within the CQV Workstream, will be responsible for supporting the timely completion of all assigned execution deliverable.

Key Accountabilities:

Drive and deliver the executions of field-based Installation Verifications, Start-up/Shakedown (commissioning) and Operation Verifications of systems found within the media, buffer, washing and sterilizing CQV Workstream.  This will include:

  • Closely working with CQ execution and engineering teams to prepare detailed plan of actions to advance execution deliverables.
  • Participating in the day-to-day planning of execution activities and CQ team member assignment to execution tasks.
  • Completing all required pre-requites/preparation work for the execution in advance of planned execution activities.
  • Following up and driving the closure of all open punch list items impeding test script execution.
  • Ensuring execution results are comprehensively complied and test scripts completed following Good Documentation Practices.
  • Ensure all executed test scripts are post-reviewed, comments are resolved and post-approved.
  • Media, buffer, washing and sterilizing area equipment on the project include systems such as preparation and hold tanks, part washers and autoclaves.
  • Be proactive and remove all roadblocks that could hold up executions.
  • Ensure all assigned activities are always performed strictly following the established safety procedures and practices.
  • Other CQV related activities as deemed necessary by the CQ Manger.

Education and Experience:

  • Bachelor’s degree in engineering, preferably in the Chemical, Mechanical or Biomedical discipline
  • 3+ years of executing commissioning and qualification protocols in pharmaceutical/bio-tech industry
  • Ability to work well independently and in teams
  • Sound written and verbal Communications skills
  • Proficiency in MS Office applications

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.

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