Manufacturing and Supply
Wo Wunder
der Wissenschaft
für Patient*innen
Realität werden
Human Factors and Usability Engineer
Cambridge, Massachusetts Salary Range USD 100,500.00 - 145,166.66
Auf einen Blick:
Unsere Teams produzieren und liefern jedes Jahr über 4 Milliarden Einheiten an Medikamenten und Impfstoffen und sorgen dafür, dass jede Innovation die Menschen erreicht, die sie am dringendsten benötigen. Unsere hochmodernen Produktionsstätten, KI-gestützten Smart Factories und wegweisenden Automatisierungstechnologien setzen neue Maßstäbe – damit Behandlungen Patient*innen schneller, sicherer und nachhaltiger als je zuvor erreichen. Hier kannst Du mit Deinen Fähigkeiten, Deinen Ambitionen und Deiner Leidenschaft die Zukunft des Gesundheitswesens mitgestalten.
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.
#GD-SA
#LI-SA
#LI-Onsite
#vhd
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.
Pursue Progress. Discovery Extraordinary.
Werde Teil von Sanofi und starte mit uns in eine neue Ära der Wissenschaft – wo dein persönliches Wachstum genauso wegweisend ist wie unsere Arbeit. Wir investieren in dich, damit du weiterkommst, schneller denkst und Dinge möglich machst, die vorher undenkbar waren. Du wirst Grenzen verschieben, Gewohntes hinterfragen und smarte Lösungen entwickeln, die direkt bei den Menschen ankommen, für die wir da sind. Bereit, die Wunder der Wissenschaft zu jagen und Leben zu verbessern? Dann lass uns gemeinsam Großes bewegen – und das Außergewöhnliche entdecken.
Bei Sanofi stehen allen die gleichen Chancen offen – unabhängig von Herkunft, Hautfarbe, Religion, Geschlecht, Nationalität, sexueller Orientierung, Alter, Staatsangehörigkeit, Familienstand, Behinderung, Geschlechtsidentität, Veteranenstatus oder anderen gesetzlich geschützten Merkmalen.
Mehr Informationen über diesen Standort
Warum bei uns arbeiten?
- Wir stellen nicht nur Medikamente her – wir bewirken etwas. Unser globales Netzwerk modernster Produktionsstätten sorgt dafür, dass Patient*innen die Behandlungen erhalten, die sie brauchen – genau zur richtigen Zeit.
- Innovation treibt uns an. Von KI-gestützter Fertigung bis hin zu weltweit führenden Produktionsmethoden setzen wir neue Maßstäbe in Effizienz und Leistung.
- Hier wachsen Karrieren. Ob in der Produktion, Qualitätssicherung, Ingenieurtechnik oder in der Supply Chain– arbeitest Du mit erstklassigen Talenten zusammen, entwickelst Deine Fähigkeiten weiter und gestaltest die Zukunft der Pharmaindustrie mit.
- Wir tun, was richtig ist. Sicherheit, Nachhaltigkeit, Vielfalt, Gleichberechtigung und Inklusion stehen im Mittelpunkt unseres Handelns – für ein Arbeitsumfeld, in dem alle erfolgreich sein können.
All-In für Vielfalt
Bei Sanofi führen unterschiedliche Perspektiven zu den besten Lösungen für Patient*innen. Erfahre von Monique Vessey, unserer Leiterin der Supply Chain -Transformation, wie ihre persönliche Geschichte ihre Arbeit bei der Bereitstellung lebenswichtiger Medikamente prägt.
"Manufacturing & Supply bildet die Brücke zwischen der Wissenschaft in unseren Forschungslaboren und den Menschen und Gemeinschaften, die wir versorgen."
Brendan O’Callaghan
Executive Vice President of Manufacturing and Supply
Mehr entdecken
Karriere in Manufacturing and Supply
Entdecke wie Sanofi die pharmazeutische Produktion und Supply Chain mit modernster Technologie, digitaler Innovation und nachhaltigen Prozessen transformiert. Ergreife Deine Chance, lebensverändernde Medikamente effizient und verantwortungsvoll bereitzustellen.
Biopharma-Innovation mit McLaren Racing beschleunigen
Was haben die Formel 1 und die biopharmazeutische Industrie gemeinsam? Geschwindigkeit, Präzision und das Streben nach Exzellenz. Erfahre wie Sanofi gemeinsam mit McLaren Racing die Medikamentenentwicklung mit modernster cutting-edge-Wissenschaft revolutioniert.
Mach mit bei unserer Talent Community
Was können wir gemeinsam erreichen? Unsere Teams arbeiten an Projekten, die Menschenleben nachhaltig verändern. Registriere Dich jetzt und erhalte die neuesten Stellenangebote, sobald diese veröffentlicht werden.