Sr Materials Engineer - Neuromodulation
MedtronicAbout the role
At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.
A Day in the Life
A career at Medtronic is like no other. We’re purposeful. We’re committed. And we’re driven by our Mission to alleviate pain, restore health and extend life for millions of people. Join us as we engineer the extraordinary!
Engineers create our market-leading portfolio of innovations. Join us to make a lasting impact. Help bring the next generation of life-changing medical technology to patients worldwide. We reward you in the ways that matter most to you. Please read the section below about benefits and compensation to learn more.
Careers that Change Lives
We are currently seeking a Sr Materials Engineer - Polymers to join our Core R&D team for Medtronic Neuromodulation and Pelvic Health. This will be on a hybrid schedule with 3 days onsite in Rice Creek, Minnesota.
In this position, you will be responsible for analyzing, researching, designing, developing, and optimizing materials and their related fabrication processes for use and application in medical device structures, systems, and subsystems. You will use your Material Science knowledge with an emphasis on polymer science, materials testing, processing, manufacturing, and analysis. You will work independently under limited supervision to determine and develop approaches to solutions and deliver results. You may manage projects/processes and may act as a mentor to colleagues or direct the work of other lower-level professionals.
Responsibilities will include but are not limited to:
• Designing and conducting experiments to evaluate material properties, including chemical, mechanical, electrical, and material compatibility with processes, other materials, drugs, and the body for various applications.
• Applying principles of chemistry, physics, and material science to develop material and processing specifications.
• Developing, analyzing, and applying material property and design allowances, processing parameters and quality engineering specifications.
• Researching, testing, and developing advanced applications of materials for implantable devices, e.g., conductive polymers, biocompatible coatings, flexible substrates, and materials for drug delivery combination products.
• Analyzing and interpreting experimental results, drawing conclusions, and making recommendations.
• Collaborating with cross-functional teams, including electrical, mechanical, and systems engineers, to develop and optimize device components and ensure their successful integration.
• Contributing to the completion of work group objectives by building relationships and reaching consensus.
• Material analyses that may include failure analysis of components, systems and subsystems, life predictions, and definition of specifications and requirements.
• Supporting the regulatory submission of both implantable and non-implantable Medtronic products.
• Supporting evaluation of hazardous substances and materials of concern in scope of various industry and international regulations
• Supporting biological evaluations per ISO 10993 and similar standards which may include developing materials-based evidence and rationales to support biological safety for change management.
Must Have: Minimum Requirements
To be considered for this role, please ensure the minimum requirements for education and experience are evident on your resume.
• Bachelors degree in a technical discipline required
• Minimum of 4 years of relevant experience, or advanced degree with a minimum of 2 years of relevant experience
Nice to Have
• Advanced degree in Material Science, Chemical Engineering, Chemistry, Polymer Science, Biomedical Engineering with Materials focus on polymer chemistry, polymer physics, or similar
• Four years of R&D materials engineering experience
• Experience with polymer materials processing, manufacturing, testing, characterization, and analysis, within a regulated industry.
• Experience in biomaterials within the medical device industry, specifically polymers.
• Experience evaluating biostability and biocompatibility, specifically of implantable medical devices, and a familiarity with relevant international standards.
• Experience with drug delivery, combination products, and material-pharmaceutical interactions.
• Experience using Design of experiments (DOE), Gage R&R analyses, six-sigma a
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