- Meta (Redmond, WA)
- …You will also have cross-functional duties with optomechanical engineering, materials development , device and system design, systems engineering, integration, ... facilitating the development of test plans for various leading-edge optical device concepts. You will join a highly cross-functional team tasked with concept… more
- Medtronic (MI)
- …or sales/service/engineering in the Cardiac Ablation, Cardiac Rhythm, or Implantable Medical Device Industry OR + Advanced Degree in Engineering ... sales/service/engineering in the Cardiac Ablation, Cardiac Rhythm, or Implantable Medical Device Industry **Desired/Preferred qualifications:** + IBHRE/RCES… more
- GE HealthCare (Bellevue, WA)
- …management experience is preferred. Demonstrated understanding or aptitude to understand Medical Device QMS requirements and regulatory requirements including ... manufacturing / production process control methodologies, and servicing in a medical device environment. Experience in a global working environment.… more
- Medtronic (Minneapolis, MN)
- …organization in the definition, design, development , and testing of complex medical device systems within the Pelvic Health Operating Unit. System designs ... Systems Engineer, you will be responsible for leading the development of our new tibial neurostimulator system solutions. You...and disposal. + Define and/or review requirements for implantable medical device systems that meet the expectations… 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 (Temecula, CA)
- …serve people in more than 160 countries. **About Abbott** For years, Abbott's medical device businesses have offered technologies that are faster, more ... disease, or products that help people with chronic pain or movement disorders, our medical device technologies are designed to help people live their lives… more
- Dentsply Sirona (Sarasota, FL)
- …Experience: + 5(+) years of experience in regulatory affairs, preferably in the medical device industry. + Experience with leading regulatory submissions and ... faster** - with our commitment to the best professional development . **Perform better** - as part of a high-performance,...13485, EU MDR). + Experience with software as a medical device , AI and/or medical … more
- Abbott (Pleasanton, CA)
- …and US device regulations and/or experience with EU and other international medical device regulations and submissions. + Ability to work in a highly ... full life. You'll also have access to: + Career development with an international company where you can grow...(EU MDR), and other international geographies. + Experience with medical device software requirements and software regulations.… more
- IQVIA (Orlando, FL)
- _IQVIA has an opportunity with one of the largest medical device manufacturers in the US. We welcome you to apply if interested! You will be asked to create an ... experience by collaborating with healthcare professionals and leading technical initiatives in medical device technology. You will be responsible for leading a… more
- TE Connectivity (Wilsonville, OR)
- … Medical business unit, part of the Industrial Solutions segment, offers medical device manufacturers a complete product offering and capability for minimally ... design engineers and a global presence in all key medical device hubs, we are a premier...+ Define process parameters in collaboration with engineering for development parts + Collaborate effectively with others across the… more