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Sanofi

Principal Device Engineer

Posted Yesterday
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In-Office
Cambridge, MA
147K-212K Annually
Senior level
In-Office
Cambridge, MA
147K-212K Annually
Senior level
Lead device development for medical technologies from concept to clinical readiness. Manage cross-functional teams and ensure rigorous testing for safety and performance.
The summary above was generated by AI

Job title: Principal Device Engineer

Location: 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.

Our Team:

The strategic vision of Sanofi’s Global Medical Device and Packaging organization is to lead the industry in device-mediated therapies, with the ambition to develop, launch and maintain best-in-class drug-delivery systems and connected medical devices that address patient unmet needs and improve health outcomes. Our specific mission is to support R&D and the Sanofi Commercial Business Units by delivering differentiated technology solutions that enhance the value of our drugs and vaccines and help patients (and health care providers) facilitate administration, thereby improving their quality of life and empowering them to take control of their disease. Our products and solutions sit on top of our market leading technology platforms, are user-centric, innovative, environmentally sustainable, producible in high quantities and are continuously improved to meet evolving needs.   

Innovation and new device development are critical pillars for ensuring our continued success to accomplish our missions. As Associate Director / Principal Device Engineer, Early Stage Programs you will lead device development to achieve clinical readiness and transition it to full commercial development programs.  You will be responsible for concept development of innovative medical device technologies, from ideation to proof of concept, in order to de-risk late-stage development programs and position us for the future. You will be a key member of Strategy and Innovation Early Stage team to interface with cross-functional teams as single point of contact of the program for Global Device and Packaging Unit (GDPU), solidifying business cases, building development roadmaps and mapping the new device technology solutions with program needs, and be fully responsible for leading all related design and development activities.

We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s lives. We’re also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started?

Main Responsibilities:

  • Lead and facilitate new device development and/or technology innovation based on clinical and patient needs, commercial and operational requirements and industry trends, create impactful solutions to expand Sanofi device IP portfolio and strength.

  • Lead external and internal project teams to develop new devices and product solutions

  • Lead the development of new devices and ensure rigorous testing to validate the performance and safety into the final combination products.

  • Manage required studies and impact assessment by working with internal and external partners and stakeholders to establish technical and commercial feasibility

  • Advance novel technology and product concepts to be clinical ready and create full development roadmap  

  • Embedded into cross-functional program teams serving as the single point of contact for device programs

  • Align with key stakeholders on the selected device solution to meet clinical program needs

  • Generate the integrated development plan and resource needs

  • Manage all device related development activities to ensure on-time, on-budget execution

  • Provide support and leadership in due diligence efforts involving novel device technologies

About You

Basic Requirements
  • Bachelor’s degree in engineering or life sciences

  • 7+ years of experience in combination products, medical devices, or development of complex technical products

  • Strong proficiency in device design from innovation through development

  • Proven experience as a technical lead on device development projects

  • In-depth knowledge of design and systems engineering of mechanical and/or electromechanical products

  • Experience working with research and clinical development teams, with a solid understanding of related issues and challenges

  • Demonstrated success in technology development through external partnerships with third parties

  • High-level competency in SolidWorks and product design

Preferred Qualifications
  • Master’s or PhD in engineering or life sciences

  • Experience with pumps or infusion systems

  • Experience in third-party management (design partners, manufacturers, and vendors)

  • Familiarity with regulatory requirements for parenteral combination products (21 CFR Parts 4 & 820, ISO 13485, 14971 & IEC 62366)

  • Strong knowledge of the US/EU external device-mediated drug delivery technology innovation ecosystem

Key Soft Skills
  • Strong leadership, communication, and presentation skills

  • Ability to capture unmet needs and translate them into product requirements

  • International business experience leading multicultural and/or multinational teams

  • Play-to-win mindset with a proactive approach

  • Extensive experience influencing and making rapid decisions in matrix and governance-driven environments

  • Attention to detail with meticulous planning

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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Pursue progress, discover extraordinary

Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.

At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.

Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!

US and Puerto Rico Residents Only

Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally inclusive and diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; natural or protective hairstyles; 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.

North America Applicants Only

The salary range for this position is:

$147,000.00 - $212,333.33

All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs. Additional benefits information can be found through the LINK.

Top Skills

Solidworks

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