Manufacturing Excellence Coordinator – VIE Contract (W/M)

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City : Toronto

Category : Contingent Worker, Manufacturing

Industry : Pharmaceutical

Employer : Sanofi

iMove, the Sanofi VIE Program, is available to citizens of the European Economic Area (EU + Norway, Liechtenstein and Iceland) aged between 18 and 28.

PLEASE NOTE that since this program is primarily an international development program, candidates cannot apply to a VIE assignment in their own country of citizenship.

PLEASE NOTE that applications that are only submitted in French cannot be considered by our non-French speaking partners at Sanofi worldwide.

Therefore, only applications that are submitted in English will be considered.

At Sanofi diversity and inclusion is foundational to how we operate and is embedded in our Core Values. We respect the diversity of our people, their backgrounds and experiences. 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 employees, patients and customers.

We are looking for a candidate for a VIE mission of:

Manufacturing Excellence Coordinator - VIE Contract (W/M)

Responsibilities:

- Supporting the implementation of Sanofi Manufacturing Systems:

  • Supporting and maintain the governance process to evaluate adherence and maturity to program
  • Leveraging daily management systems and fast resources to drive continuous improvement in manufacturing operations
  • Participating in the Sanofi Lean Network and the North American working group

- Providing support and direction for Operational Excellence program implementation:

  • Supporting IO (Industrial Operations) groups to identify continuous improvements initiatives
  • Facilitating and leading implementation of improvement with cross-functional teams
  • Preparing with the functional team and presenting to management a clear and convincing justification and timeline for proposed changes
  • Applying consistently and effectively the continuous improvement principles

- Assisting IO groups to standardize methods for the definition of resources and capacity:      

  • Improving flows of materials, products and documentations and information
  • Stabilizing processes to reduce exceptions that impact throughput and quality
  • Increasing the labour yield within IO

Requirements:

  • Master degree in Business (Operations), Science, Engineering or other relevant technical discipline
  • 2-5 years of manufacturing experience with good understanding of overall business operations knowledge
  • Demonstrated experience in LEAN or Six Sigma concepts and principles (Deployment, Mapping, Change Management, Project Management, etc.)
  • Systematic problem-solving capabilities using appropriate process improvement methodologies to analyse complex data/information from cross-functional teams, both locally and globally
  • Working knowledge of GMP (Good Manufacturing Practices) and regulatory agencies (i.e. FDA (Food and Drug Administration) etc.)
  • Strong scientific and analytical understanding of processes and quality systems
  • Excellent written and verbal communication, interpersonal and presentation skills
  • Ability to work cross-functionally
  • Advanced Excel
  • Strategic planning in analysis, “can do” attitude, open minded, agility to adapt to the diverse environment, rigorous, autonomous, and proactive
  • Very good English, should feel comfortable while publicly speaking in English

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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