Senior New Product Develpment Engineer

TE Connectivity's Sensors business unit is seeking a talented Senior NPI Product Development Engineer with a strong background in medical device development to join our high-performing product development team in Galway. This is a dynamic role where you will collaborate with global cross-functional teams including product management, sales, manufacturing, and operations to drive innovation and ensure the successful delivery of market-leading medical sensor solutions.

You will play a key role in the design, development, and implementation of cutting-edge medical sensors, bringing original concepts into practical application. The ideal candidate is a proactive problem-solver, technically skilled, and experienced in navigating complex stakeholder environments to deliver profitable outcomes.

Why Join Us?

At TE Connectivity, we offer more than just a job — we provide an opportunity to make a real impact in healthcare through technology. You’ll join a supportive and forward-thinking team working on products that truly make a difference in patients' lives. Enjoy a collaborative culture, continuous learning, and exciting career growth opportunities.

Your responsabilities will include:

• Lead the end-to-end development of medical sensors, including 3D modeling, design documentation, DFMEA, and requirements management.

• Create and maintain comprehensive product documentation such as 2D/3D production drawings, specifications, test protocols, technical reports, and design verification records.

• Conduct and lead design reviews, ensuring alignment with cross-functional project teams and key stakeholders.

• Collaborate with suppliers to qualify components and materials, ensuring high standards of quality, reliability, and compliance.

• Support risk assessments, including process and design FMEAs.

• Perform feasibility studies and implement improvements in manufacturing processes to enhance product quality and efficiency.

• Contribute to continuous improvement and innovation initiatives within the R&D organization.

• Ensure compliance with relevant regulatory standards and medical device quality systems.

What your background should look like:

• Master’s degree in Mechanical Engineering, Electrical Engineering, or a closely related discipline.

• Minimum of 3 years of professional experience in product design, preferably within the medical device industry.

• Proven experience in design for manufacturing (DFM) and working within regulated environments.

• Solid understanding of medical quality systems and standards (e.g., ISO 13485).

• Strong communication skills in English (C1 level), with the ability to work effectively across global teams.

• Proficiency in CAD tools for 3D modeling and drawing development.

• Background in biocompatibility for surface-contact medical devices.

• Experience working in the mechatronics or sensor technology industry.

• Certification in Design for Six Sigma (DFSS) or similar methodologies.

  
  

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