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Associate Director, Human Factors & Usability Engineering, Cambridge
Client: Sanofi
Location: Cambridge, United Kingdom
Job Category: Other
EU work permit required: Yes
Job Reference: 01263bc60585
Job Views: 3
Posted: 18.07.2025
Expiry Date: 01.09.2025
Job Description:
Job title: Associate Director, Human Factors & Usability Engineering
Location: Cambridge, MA, Morristown, NJ
About the job
We deliver 4.3 billion healthcare solutions to people every year, thanks to the meticulous planning of our Manufacturing & Supply teams. With your talent and ambition, we can do even more to protect people from infectious diseases and bring hope to patients and their families.
At Sanofi, we chase the miracles of science to improve people's lives. We offer a dynamic environment for career growth, exploring opportunities, and pushing the boundaries of what's possible.
Role Overview:
The Associate Director will lead HFUE activities, improve HFUE processes, drive user-centric design, optimize product UI, ensure product safety and effectiveness, and enhance user experience across the pipeline. Drive HFUE initiatives in early, development, and LCM projects, ensuring strategic and rigorous execution and timely delivery.
Main Responsibilities:
* Lead human factors and usability engineering activities throughout product lifecycle
* Ensure product safety, effectiveness, and optimal user-interface design
* Drive user-centered design processes supporting Sanofi's product pipeline
* Collaborate with cross-functional teams to implement HFE best practices
* Oversee regulatory compliance and documentation
This role offers the opportunity to shape the future of medical device usability while working with cutting-edge technology with a global healthcare leader.
About You
* Strategic thinking and risk-based decision making
* Agile leadership mindset
* Critical problem-solving abilities
* Excellent communication and collaboration skills
Technical Expertise:
* Implementation of HFUE processes: user needs identification, requirements generation, context of use, risk controls assessment, execution, study design, deliverable management, regulatory documentation
Required Qualifications:
* Bachelor's or Master's in Human Factors Engineering, Biomedical Engineering, Biomechanics, Mechanical Engineering, Behavioral Sciences, Psychology, Industrial Design, or related field
* Extensive experience in pharmaceutical or medical device industry
* Deep knowledge of combination products and human factors
* Strong understanding of FDA Guidance, Standards, and Regulations
Preferred Experience:
* Wide range of FDA submission experience
Why Choose Us?
* Bring science to life with a supportive, future-focused team.
* Opportunities for growth and international mobility.
* Rewarding benefits including healthcare, wellness, and parental leave.
Sanofi is committed to diversity and equal opportunity employment. All qualified applicants will receive consideration without regard to race, color, religion, sex, national origin, age, disability, or other protected characteristics.
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Pursue, discover
Better medications, outcomes, and science are out there. Progress depends on diverse people united by a desire to make miracles happen. Join us.
We provide equal opportunities to all, regardless of race, color, religion, sex, national origin, age, or gender identity.
Check out our Diversity, Equity, and Inclusion actions!
The salary range for this position is: $147,000.00 - $212,333.33
All compensation will be based on experience. Additional benefits are available.
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