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Project Manager Bulk Processing/Validation

North York - Ontario - Canada - Life Sciences & Health Care - Pharmaceutical - Regulatory - Academic Bachelor

Our client is seeking a dedicated a Project Manager Bulk Processing/Validation to join their reputable pharmaceutical company in Toronto, Ontario. They are offering a competitive compensation package, a collaborative work environment and an excellent work/life balance. Apply now if you are interested in this exciting and challenging full-time position.

Feel free to contact

Diana Grodowski, Account manager

Apply now

Job description


Our client is seeking a dedicated Project Manager Bulk Processing/Validation to develop strategy, plan and lead activities related to process improvement (including raw material change) and/or process validation projects to support Bulk Industrial Operations. Provide scientifically sound analysis, discussions and recommendations when appropriate

Position Summary:

  • Support specific licensed product/process through the scientific and technical continuous improvement of the existing manufacturing process and support production on a daily basis to reach industrial excellence;
  • Ensure robustness and continuous improvement of manufacturing processes;
  • Strengthen process and product knowledge through trending analysis, process criticality analysis, presence at the shop floor and technical assistance to current manufacturing processes. Stay abreast of current advances in area of technical expertise;
  • Drive or support troubleshooting/investigation related to his/her products/process. Support manufacturing for complex issues, product impact assessment, root cause analysis;
  • Contribute to strategy related to specific project, process validation, scientific and technological assessment and inspection readiness. Drive or support the implementation of actions plans;
  • Share knowledge and area of expertise to support business. Lead or participate on Project Teams, as MTech representative. Interface with other MTech areas and other departments (e.g. Bulk Manufacturing teams, QO Validation, QO Shop Floor, QC, GEM, R&D, RA) for assistance;
  • Contribute to maintain compliance with all cGMP regulatory standards and Sanofi Pasteur policies and procedures. Contribute to quality improvements and participate in inspection and regulatory responses.







About you

Our client is seeking a Project Manager Bulk Processing/Validation with the following Education and experience: 

Specific degree, duration of experience (minimum): BSc (Science/Engineering) with 5 years related experience or MSc (Science/Engineering) with 3 years related experience.


  • Strive for results (be achievement-oriented to positively impact project performance), Cooperate transversely (collaborate effectively across the organization), Commit to costumers (deliver solutions aligned with customer needs), Make decisions (make choices to positively impact business results);
  • Key technical competencies and soft skills: Knowledge of 1 or more technical areas of manufacturing (fermentation, cell culture, purification), project management.



What we offer

Brunel Life Sciences provides global staffing, recruitment, and contracting solutions for Life Sciences, Pharmaceutical, Biotechnology and Healthcare organizations. Brunel Life Sciences plays a vital part of the Brunel International Group, with over 100 offices in 40 countries and approximately 13,000 employees around the globe.

About us

Our client is an innovative multinational pharmaceutical company. They are creators of breakthrough treatments and healthier alternatives to improve the quality of life for people, animals and communities.


  • Vacancy number: PUB151522
  • Location: North York
  • Market: Life Sciences & Health Care
  • hours per week: 35.0
  • Branche: Pharmaceutical
  • Education level: Academic Bachelor
  • Area of Expertise: Regulatory
  • Closing date: Sunday, March 25, 2018
Apply now

Feel free to contact


Diana Grodowski

Account manager Brunel Canada Toronto

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