Fabrication et Approvisionnement
Là où les miracles
de la science
deviennent une réalité pour les patients
Human Factors and Usability Engineer
Cambridge, Massachusetts Salary Range USD 100,500.00 - 145,166.66
En bref
Nos équipes produisent et livrent chaque année plus de 4 milliards de médicaments et de vaccins, veillant à ce que chaque avancée soit accessible à ceux qui en ont le plus besoin. Grâce à des infrastructures ultra-modernes, des usines intelligentes pilotées par l’IA et une automatisation de pointe, nous repoussons les limites pour garantir que nos traitements parviennent aux patients plus rapidement, en toute sécurité et de manière plus durable que jamais. C’est ici que votre expertise, votre ambition et votre passion peuvent façonner l’avenir de la santé.
Job title: Human Factors and Usability Engineer
Location: Cambridge, MA / Morristown, NJ
About the job
Join a global network that powers how Sanofi delivers — seamlessly, purposefully, and at scale. In Manufacturing & Supply, you’ll help reimagine how life-changing treatments reach people everywhere, faster.
Our Purpose & Team:
GDPU is a global business unit in M&S which develops and maintains Sanofi's parenteral injection systems including Insulin Pens, Autoinjectors, Large Volume Devices, infusion systems, and Pre-Filled Syringes. The unit is a project-centric organization executing development and lifecycle management (LCM) projects of drug delivery devices for mAbs, vaccines, peptides, genomics, and more, and supports device product maintenance post-launch.
The Human Factors & Usability Engineer will support GDPU HF/UE activities for medical devices, combination products, and medicinal products as applicable across our deep pipeline from early engagement through lifecycle management. This role operates with meaningful autonomy while benefiting from mentorship and oversight that supports professional growth and development.
Responsibilities span the full HF/UE lifecycle from early-stage generative research and user characterization through formative evaluation, iterative design support, and summative validation with contributions to user needs analysis, user requirements development, task analysis, use-related risk analysis, user interface (UI) design support, and usability study execution.
Our team supports our mission to make the impossible possible by delivering best-in-class and first-in-class products, working together to define user needs and establish user requirements that meet the unmet needs of patients, and ensuring a user-centric approach to informing the user-interface design of our products. Ultimately, we are committed to ensuring our products meet the needs of users, reducing use-related issues, optimizing user interface design to support safe and effective use, improving overall usability, and enhancing the patient experience.
About Sanofi
We’re an R&D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people’s lives.
Main Responsibilities:
Conduct early-stage generative research (ethnographic methods, contextual inquiry, participatory design) to discover user needs, contexts of use, and unmet needs
Execute user characterization studies to systematically explore the capabilities, limitations, and variability of intended user populations, including those with physical, sensory, or cognitive impairments, to ensure findings inform appropriate user requirements, UI specifications, and design decisions for safe and effective use
Perform functional task analysis, use-related hazard analysis, and known use problems analysis to inform use-related risk analysis and identify, assess, and prioritize use-related risk controls and mitigation strategies
Apply good study design to enable iterative UI design leveraging a range of research and testing methods to lead or conduct formative research including heuristic evaluations, cognitive walkthroughs, iterative labeling testing, and sprint studies
Conduct use error analysis and root cause analysis to distinguish design-induced errors and inform UI design improvements
Translate study results and technical constraints into user needs, design recommendations, and UI specifications
Develop study protocols and execute summative validation studies to demonstrate safe and effective use
Apply instructional and visual design principles to develop Instructions for Use (IFU), labeling, and patient support program content
Support regulatory submissions and health authority interactions (FDA, EMA, Notified Bodies, NMPA) under direction of the Global Head of HFUE
Collaborate with cross-functional teams (design, regulatory, clinical, quality, marketing) as the HF/UE representative
Support vendor and consultant activities for usability study execution
Contribute to HF/UE process improvements, tools, and knowledge sharing initiatives
About You
Basic Qualifications:
Education: Bachelor's degree in human factors, psychology, biomedical engineering, or related field (e.g., cognitive science, engineering sciences, human-computer interaction)
Experience: 2.5 to 5 years applying human factors engineering to medical devices or combination products
Health Authority & Standards knowledge: all relevant FDA HF Guidance documents, IEC 62366-1:2015+A1:2020, ISO 14971:2019, ISO 13485, EMA guidelines
Experience designing and executing generative, formative, and summative usability studies
Strong cross-functional collaboration and communication skills (written and spoken English)
Ability to work autonomously, seek guidance when needed, and thrive within a matrix organization with mentorship support
Willingness to travel to study sites (up to 20%)
High self-motivation and passion for human factors and patient-centered design
Preferred Qualifications:
Master's degree in human factors or related field
Proficiency in user-centric design principles and tailored application of HF principles through systematic, risk-based, fit-for-purpose, tailored processes aligned with latest FDA expectations and relevant FDA Guidance documents
Experience moderating usability tests and managing external vendors
Knowledge of instructional design and package/labeling design for medical devices
Experience with health authority submissions and regulatory interactions (FDA, EMA, Notified Bodies)
Understanding of drug-device development lifecycle, change control, and LCM processes
Ability to analyze qualitative and quantitative data, including basic statistics
Familiarity with design and prototyping methods and tools
Why Choose Us?
Bring the miracles of science to life alongside a supportive, future-focused team.
Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally.
Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave.
Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.
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All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs, and additional benefits information can be found here.
Toujours Progresser. Découvrir l’Extraordinaire.
Rejoignez Sanofi et entrez dans une nouvelle ère de la science – où votre parcours peut être aussi transformateur que le travail que nous accomplissons. Nous investissons en vous pour que vous alliez plus loin, accélériez votre réflexion et accomplissiez ce qui n’a jamais été fait auparavant. Vous contribuerez à repousser les limites, à bousculer les conventions et à concevoir des solutions plus intelligentes pour les communautés que nous servons. Prêt·e à poursuivre les miracles de la science et à améliorer la vie des gens ? Poursuivons le progrès et découvrons l’extraordinaire – ensemble.
Chez Sanofi, nous croyons dans l’égalité des chances, sans distinction de race, de couleur, d’ascendance, de religion, de sexe, d’origine, d’orientation sexuelle, d’âge, de citoyenneté, d’état civil, de handicap, d’identité de genre ou de tout autre critère protégé par la loi.
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Pourquoi nous rejoindre ?
- Nous ne faisons pas que fabriquer des médicaments—nous créons un impact. Grâce à notre réseau international d’installations de pointe, nous veillons à ce que les patients reçoivent les traitements dont ils ont besoin, au moment où ils en ont besoin.
- L’innovation est notre moteur. De la fabrication pilotée par l’IA aux méthodes de production inédites, nous repoussons les limites de l’efficacité et de la performance.
- Ici, vous évoluez. Que ce soit en production, en qualité, en ingénierie ou en supply chain, vous collaborerez avec des experts de renom, développerez vos compétences et contribuerez à façonner l’avenir de l’industrie pharmaceutique.
- Nous faisons ce qui est juste. Sécurité, durabilité, diversité, équité et inclusion sont au cœur de notre engagement, garantissant un environnement où chacun peut s’épanouir.
Tous engagés pour la diversité
Chez Sanofi, la diversité des perspectives est une source d’innovation au service des patients. Découvrez Hamza Laajaj, Chef de projet déploiement applicatif à Neuville-sur-Saône, et son engagement pour un environnement inclusif où chaque voix compte. Pour lui, c’est en embrassant la diversité que nous libérons l’innovation et repoussons les limites de la santé.
"Nous faisons ce qui est juste. Sécurité, développement durable, diversité, équité et inclusion sont au cœur de notre engagement, garantissant un environnement où chacun peut s’épanouir."
Brendan O’Callaghan
Executive Vice President of Manufacturing and Supply
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