Manufacturing Technology Process Improvement Scientist - VIE Contract (W/M)

Sanofi - Toronto, ON (30+ days ago)

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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 Technology Process Improvement Scientist - VIE Contract (W/M)

Responsibilities:
Designing, planning and coordinating experiments, scaling-up and scaling-down manufacturing processes with the goal of capacity increase manufacturing or process robustness
Contributing to trouble-shooting, support problem-solving and data analysis from execution of studies
Being accountable for detailed validation and study documentation (protocols, reports, URS (User Requirement Specification)) related to process
Supporting cleaning/decontamination studies where required
Ensuring documentation is compliant with Sanofi Pasteur policies and regulatory expectations
Participating in project teams, working groups
Interacting with cross functional teams in Production, Quality operations, Engineering, RA (Regulatory Affairs), R&D (Research & Development) to support process and technology transfer, scale-up, process improvement, validation and regulatory submission
Proposing / implementing innovative methodologies / technologies into the laboratory / manufacturing process
Standardizing experimental procedures/ equipment operation procedures / analysis methodologies, and training others on these

Requirements:
Master degree or higher in: Biology, Microbiology, Fermentation or related Engineering degree
1 year of related working experience is required
Laboratory experience would be a big plus
Knowledge of 1 or more technical areas of manufacturing (fermentation, cell culture, purification) would be a plus
Strive for results (be achievement-oriented to positively impact project performance)
Cooperate transversally (collaborate effectively across the organization)
Commit to costumers (deliver solutions aligned with customer needs)
Make decisions (make choices to positively impact business results)
Proficiency in MS Office Suite and Data Analysis Software
Languages: Fluent 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.