Senior Engineer, Medical Device
Listed on 2026-02-28
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Engineering
Biomedical Engineer, Medical Device Industry, Product Engineer
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and Med Tech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
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R&D Product Development
Job Sub FunctionBiomedical Engineering
Job CategoryScientific/Technology
All Job Posting LocationsRaritan, New Jersey, United States of America
Job Description About SurgeryFueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments. Are you passionate about improving and expanding the possibilities of surgery? Ready to join a team that’s reimagining how we heal? Our Surgery team will give you the chance to deliver surgical technologies and solutions to surgeons and healthcare professionals around the world.
Your contributions will help effectively treat some of the world’s most prevalent conditions such as obesity, cardiovascular disease, and cancer. Patients are waiting. Our business offers a broad range of products and technologies, including surgical staplers, clip appliers, trocars and sealing devices—that are used in a wide variety of minimally invasive and open surgical procedures. Your unique talents will help patients on their journey to wellness.
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Johnson & Johnson Med Tech is currently recruiting for a Senior Medical Device Engineer
. The position is located in Raritan, NJ and will work a Flex/Hybrid schedule with 3 days per week on-site.
- Provide technical support to multidisciplinary project teams in the design, development, manufacturing, and commercialization of medical devices in the cardiovascular space.
- Serve as a Technical Leader, and/or Subject Matter Expert for one or more projects and/or technical areas.
- Support and/or lead exploratory R&D, new product development, product line extensions, and existing product improvements.
- Identify user needs via customer interactions (VOC – Voice of Customer) and translate them into customer requirements, design requirements, and detailed specifications.
- Perform detailed design, material selection and engineering analysis including creation and revision of 3D models and technical drawings.
- Conduct Design for Manufacturing and Assembly (DFMA) analyses.
- Build and assemble prototype devices for activities such as VOCs, concept testing and optimization, preclinical studies, test method development, and bench‑top testing.
- Support and/or lead Design Control activities such as strategies, design verification and validation, technical and design reviews, documentation, and Design History Files.
- Work effectively both face‑to‑face and remotely on internal and external cross‑functional project teams.
- Identify new innovation opportunities and secure appropriate intellectual property.
- Communicate business‑related issues or opportunities to the next management level.
- Following all company guidelines related to health, safety and environmental practices.
- Ensure personal and company compliance with all federal, state, local and company regulations, policies, and procedures.
- Perform other duties as assigned.
- Bachelor’s degree with 4+ years’ experience or an advanced degree with 3+ years’ experience in medical device research or product development experience required.
- Experience in open and minimally invasive procedures and related medical devices in the cardiovascular space is required.
- Track record of innovation in developing new products and processes and/or improving existing ones is required.
- Demonstrated knowledge and experience in medical device design & development and regulations is required.
- Strong CAD capability required.
- Hands‑on experience of part/assembly design and drafting, including standard methodologies for dimensions, tolerances, specifications, and notes is required.
- Ex…
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