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Lead-Human Factors Usability Engineering

Cambridge, Massachusetts Permanent 发布日期 Aug. 28, 2024
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Cambridge, MA

About the Job

We deliver 4.3 billion healthcare solutions to people every year, thanks to the flawless planning and meticulous eye for detail 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.

Your job, as Human Factors Usability Engineering Leaderwithin our Drug Product and Device group, will be to contribute Human Factors Engineering (HFE) in our development projects (medical devices or combination products) and to ensure that HFE tasks are performed with appropriate rigor and in a timely manner.

We arean innovative global healthcare company with one purpose: to chase the miracles ofscience to improve people’s lives.We’realso a company where you can flourish and growyour career, with countless opportunities to explore, make connections with people, andstretch the limits of what you thought was possible. Ready to get started?

Main Responsibilities

  • Develop user needs together with patients, user, and patient/user associations.

  • Design the product to meet users' needs and customer expectations.

  • Ensure the product is safe and effective to use and complies with applicable regulations worldwide.

  • Translate insights from exploratory and formative evaluations into user interface specifications and provide user insights to the design team.

  • Provide human factors engineering subject matter expertise to cross-functional global teams, interacting with experts in industrialization, clinical operations, business, marketing, medical, and regulatory affairs.

  • Oversee and participate in design validation and verification activities, including developing protocols, conducting validation testing, reviewing validation reports, and developing engineering reports for regulatory submissions.

About you:

  • Bachelor’s degree in human factors/usability or a related field (e.g., biomedical engineering, mechanical engineering, psychology, economics, human-computer interaction, etc.).

  • Master’s degree in human factors/usability or a related field (e.g., biomedical engineering, mechanical engineering, psychology, human-computer interaction) preferred, but not required.

  • 5+ years of work experience applying human factors to medical devices or combination products.

  • Strong understanding of human factors research elements (e.g., study design, moderating, root cause analysis).

  • Familiarity and comfort with navigating health authority expectations for human factors.

  • Deep knowledge of human factors/usability engineering principles, best practices, and international usability standards and guidance (e.g., ANSI/AAMI/IEC 62366-1, ANSI/AAMI HE75, FDA guidance, NMPA guidance, ISO 14971).

  • Willingness to travel regularly to human factors study sites, primarily in the US, or to Europe or Asia.

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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追寻 发展探索 菲凡

进步需要我们每个人的参与——不论其背景、地域、或职业,我们都有一个共同的愿望:创造奇迹。你也可以成为其中的一员。我们不断追求变革,拥抱新思想,探索我们所能提供的一切机会。让我们一起追求进步。共同发现非凡。

在赛诺菲,不分种族、肤色、血统、宗教、性别、国籍、性取向、年龄、公民身份、婚姻状况、残疾或性别认同,我们为所有人提供平等的机会。

观看 “在赛诺菲的一天” ,并在官网 (sanofi.com) 上查看赛诺菲的多元化、公平与包容倡议!

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实验室里的女人通过放大镜观察小瓶

在美国的职位

加入我们的美国团队。我们将为您提供专家指导和培训平台,从而帮助我们营造良好的企业文化。我们鼓励您以饱满的热情和充沛的精力投入到工作中,然后发挥自身能力推进药物和疫苗的研发,同时将研发到临床治疗的时间减半。

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