- JBT Corporation (Eastlake, OH)
- …Grow with Excellence, and Advance with Innovation . The Opportunity As our Controls Engineer , you will report to the Controls Manager. On a given day, you may: ... electrical devices and system. + Conduct electrical/hydraulic/pneumatic design, peripheral device programming, machine PLC programming, coordinate the machine debug,… more
- Capgemini (Burlington, MA)
- …verification strategies, manage a team of engineers, and ensure compliance with medical device regulations. **Your Role** . Lead Verification Strategy: Develop ... systems. . Compliance & Standards: Ensure all verification activities align with relevant medical device regulations such as ISO 13485, IEC 62304, and FDA… more
- Abbott (Scarborough, ME)
- …years of technical work experience in precision injection molding, preferably in the medical device industry. + Knowledge of mold design fundamentals, molding ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more
- Medtronic (Louisville, CO)
- …in Continuous improvement projects + Experience in validation (MVP/IQ/OQ/MSA/PQ) in a medical device environment + Knowledge of GD&T and problem-solving tools: ... future generations live better, healthier lives. As a Manufacturing Engineer at Medtronic's Louisville, CO facility, you'll play a...to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference… more
- Medtronic (Minneapolis, MN)
- …and external regulatory agencies + High attention to detail and accuracy + Medical device experience strongly preferred **Physical Job Requirements** The above ... area of new product development, the Senior Supplier Quality Engineer will be required to drive multiple aspects of...to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference… more
- DEKA Research & Development (Manchester, NH)
- …for a Verification and Validation Test Engineer to work in a dynamic medical device R&D environment. Test Engineering is a high-visibility role with ... knowledge of FDA Quality System Regulations (QSRs) and/or ISO 13485, and other medical device industry experience preferred About DEKA: One hour from the… more
- DEKA Research & Development (Manchester, NH)
- …in Manchester, NH, is seeking a Senior Test Engineer to work in a dynamic medical device R&D environment. This is a high visibility role with a direct ... you will make an impact as a Senior Test Engineer : + Writing test plans, test procedures and other...Quality System Regulations (QSRs) and/or ISO 13485, and other medical device industry experience + Experience with… more
- Medtronic (Boston, MA)
- …framework + Experience developing for Windows applications **Nice to Have:** + Medical Device Experience + Experience developing software for commercial ... of professional growth and cross-functional collaboration as we work together to engineer the extraordinary.** ** ** **You Will:** + **** Create and maintain… more
- Medtronic (Northridge, CA)
- …radio firmware and Bluetooth Low Energy (BLE) stack, ensuring compliance with the medical device standards. Design and implement the Radio Frequency (RF) ... - 12 Nov 2025 **Position Description:** Sr. Embedded Software Engineer for Medtronic, Inc. located at Northridge, CA. Collaborate... SDLC standard and IEC 62304 within the regulated medical device industry; Embedded Linux RTOS environments… more
- Medtronic (Milwaukee, WI)
- …at least two (2) years' experience with each of the following: Manufacturing in medical device industry including Class I, Class II and Class III devices; ... on - 23 Oct 2025 Position Description: Sr. Manufacturing Engineer for Medtronic, Inc. located in Milwaukee, WI. Responsible...waste reduction and inventory control; NC & CAPA Investigations; Medical Device Quality & Regulatory Compliance (FDA… more
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