- Medtronic (Minneapolis, MN)
- …the following tasks: + Product Security - Implement security requirements across the medical device development lifecycle by collaborating with teams to uphold ... and the use of Hardware Security Modules (HSMs) for medical device protection. + Use of advanced...device software and systems + Security Standards & Compliance - Ensure the implementation and maintenance of security… more
- Hologic (Newark, DE)
- …impact on healthcare innovation. **Knowledge:** + Deep understanding of global medical device software regulations, including FDA 21 CFR Part 820, EU ... about ensuring the quality, safety, and reliability of life-saving medical device software? Hologic is seeking a...ability to lead design assurance efforts for software in medical devices, ensuring compliance and safety throughout… more
- Terumo Medical Corporation (Elkton, MD)
- …TMC is part of Tokyo-based Terumo Corporation; one of the world's leading medical device manufacturers with $6+ billion in sales, 30,000+ employees worldwide ... Dec 1, 2025 Req ID: 5359 Location: Elkton, MD, US Company: Terumo Medical Corporation Department: VS Peripheral Management Terumo Medical Corporation (TMC)… more
- J&J Family of Companies (Irvine, CA)
- …for disruptive innovation that positions our organization at the forefront of medical device technology. The Senior Principal Engineer leadership will ensure ... Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where...discipline. Master's or PhD preferred, with a focus on medical device development, materials science, or related… more
- Globus Medical, Inc. (KS)
- …Service Engineer in a technical customer service/field service role; experience in the medical device industry preferred + Experience with GMP and ISO standards ... At Globus Medical , we move with a sense of urgency...the needs of these patients, and the surgeons and healthcare providers who treat them. We embrace a culture… more
- Integra LifeSciences (Plainsboro, NJ)
- …corporate policies, US Food and Drug Administration regulations, ISO 9001, ISO 13485, the Medical Device Directive, the Canadian Medical Device ... work that creates change and shapes the future of healthcare . Thinking differently is what we do best. To...and Drug Administration (FDA) regulations, ISO 9001, ISO 13485:2003, Medical Device Directive (MOD), the Canadian … more
- Veterans Affairs, Veterans Health Administration (Orlando, FL)
- …and safety alert program for medical devices, including medical device incident investigations to assure compliance with patient safety goals, Safe ... for patient care activities. The supervisory biomedical engineer (clinical) is responsible for compliance and reporting of medical device , cyber security,… more
- Medtronic (Toledo, OH)
- …in servicing medical personnel on product use + Experience with a medical device company or pharmaceutical company, and clinical experience in a specialty ... 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… more
- Terumo Medical Corporation (Elkton, MD)
- …TMC is part of Tokyo-based Terumo Corporation; one of the world's leading medical device manufacturers with $6+ billion in sales, 30,000+ employees worldwide ... Req ID: 4974 Location: Elkton, MD, US Company: Terumo Medical Corporation Department: PM&PD Management Terumo Medical ...broad range of applications for numerous areas of the healthcare industry. TMC places a premium on providing customers… more
- Abbott (Plymouth, MN)
- …support processes. In this role, you will also be responsible for performing medical device regulatory reporting in accordance with global regulatory guidelines, ... authorities. **What You'll Work On** + Independently determining and filing appropriate medical device regulatory reports with various regulatory agencies and… more