[Only 24h Left] Associate Director-Principal Engineer, New Device Technology Programs Position Available In Morris, New Jersey

Job Description:

Job Title:

Associate Director-Principal Engineer, New DeviceTechnology Programs Location:

Cambridge, MA, Morristown, NJ, Aboutthe Job We deliver 4.3 billion healthcare solutions to people everyyear, thanks to the flawless planning and meticulous eye for detailof our Manufacturing & Supply teams. With your talent and ambition,we can do even more to protect people from infectious diseases andbring hope to patients and their families. The strategic vision ofSanofi’s Global Medical Device and Packaging organization is tolead the industry in device-mediated therapies, with the ambitionto develop, launch and maintain best-in-class drug-delivery systemsand connected medical devices that address patient unmet needs andimprove health outcomes. Our specific mission is to support R Dand the Sanofi Commercial Business Units by deliveringdifferentiated technology solutions that enhance the value of ourdrugs and vaccines and help patients (and health care providers)facilitate administration, thereby improving their quality of lifeand empowering them to take control of their disease. As AssociateDirector/Principal Engineer of New Device Technology InnovationPrograms, you will drive innovative new device technologydevelopment to achieve clinical readiness and transition it to fullcommercial development programs. You will be a key member of NewDevice Technology Research, Technology Innovation and ExternalCollaboration team to interface with cross-functional, initiatingnovel concepts development, establishing proof-of-concept,solidifying business cases, building development roadmaps andmapping the new device technology solutions with program needs, andbe fully responsible for leading all related developmentactivities. We are an innovative global healthcare company with onepurpose: to chase the miracles of science to improve people’slives. We’re also a company where you can flourish and grow yourcareer, with countless opportunities to explore, make connectionswith people, and stretch the limits of what you thought waspossible. Ready to get started? Main Responsibilities

• Lead andfacilitate device technology innovation and development based onclinical and patient needs, commercial and operational requirementsand industry trends, create impactful solutions to expand Sanofidevice IP portfolio and strength
• Work with new device technologyresearch team to evaluate new device technology and productsolutions About You Basic Qualifications
• BS degree in mechanical,electrical or biomedical engineering or adjacent discipline and 10years’ work experience in combination product or medical devicedevelopment, or MS/PhD in mechanical, electrical or biomedicalengineering or adjacent discipline with 7 years related workexperience.
• Prior experience working with research and clinicaldevelopment teams; solid understanding of related issues andchallenges.
• Strong knowledge of the US/EU externaldevice-mediated drug delivery technology innovation eco-system.
• Solid experience and knowledge of technology development throughexternal partnership with third parties. Preferred Qualifications
• End-to-end product design and development experience stronglydesired.
• Experience in third party management (of manufacturersand vendors) is preferred.
• Expertise around regulatoryrequirements for parenteral combination products is preferred (21CFR parts 4 & 820, ISO 13485, 14971 & IEC 62366).

Soft skills:

• Strong leadership, communication, and presentation skills
• Capableof capturing unmet needs and translating them into productrequirements
• International business experience leadingmulticultural and / or multinational team(s)
• Play to win mindset
• Extensive experience with successfully influencing and rapiddecision making in matrix and / or governance driven environments
• Attention to details with meticulous planning
• Conduct requiredstudies and impact assessment by working with internal and externalpartners and stakeholders to establish technical and commercialfeasibility
• Advance the novel technology and product concepts tobe clinical ready and create full development roadmap
• Embeddedinto cross-functional program teams serving as the single point ofcontact of GDPU function for innovation programs
• Synthesizeprogram needs and leverage learnings from different programs,identify platform opportunity when possible
• Interface withinternal and external device development partners to align resourceand priorities to transition and support new device developmentprograms
• Align with key stakeholders on the selected devicesolution to meet clinical program needs
• Generate the integrateddevelopment plan and resource need
• Manage all device relateddevelopment activities to ensure on-time, on-budget execution
• Provide support and leadership in due diligence efforts involvingnovel device technologies Why Choose Us?
• Bring the miracles ofscience to life alongside a supportive, future-focused team.
• Discover endless opportunities to grow your talent and drive yourcareer, whether it’s through a promotion or lateral move, at homeor internationally.
• Enjoy a thoughtful, well-crafted rewardspackage that recognizes your contribution and amplifies yourimpact.
• Take good care of yourself and your family, with a widerange of health and wellbeing benefits including high-qualityhealthcare, prevention and wellness programs and at least 14 weeks’gender-neutral parental leave.

Sanofi Inc. and its U.S. affiliatesare Equal Opportunity and Affirmative Action employers committed toa culturally diverse workforce. All qualified applicants willreceive 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 militarystatus; domestic violence victim status; atypical cellular or bloodtrait; genetic information (including the refusal to submit togenetic testing) or any other characteristic protected by law.

GD-SA LI-SA

LI-Onsite vhd All compensation will be determinedcommensurate with demonstrated experience. Employees may beeligible to participate in Company employee benefit programs, andadditional benefits information can be found here.