- Abbott (San Diego, CA)
- …* Minimum 15 years of experience in software development, preferably in a medical device /diagnostics or other regulated environment. Direct experience with IVD ... * Minimum 10 years of experience in algorithm development, preferably in a medical device /diagnostics or other regulated environment. Direct experience with IVD… more
- BD (Becton, Dickinson and Company) (Durham, NC)
- …Bachelor's degree + Minimum 5 years of strong Regulatory Affairs experience in the medical device and/or in vitro diagnostic and/or regulated product field + ... Cybersecurity, Board of Pharmacy, and Environmental requirements + Working knowledge of medical device stand-alone software, device interoperability and IEC… 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...for development parts + Demonstrated problem solving skills in support of manufacturing operations + Demonstrated ability to train… more
- Abbott (St. Paul, MN)
- …Regulatory Operations team and lead portfolio management of regulatory programs across medical device business units, international regulatory teams, and global ... By applying best practices in program management, the Director will help achieve-and exceed- medical device division goals. This position serves as the primary… more
- University of Miami (Miami, FL)
- …to create high-fidelity, simulation-ready models. These models will be used to simulate medical procedures and evaluate device performance. + In Silico Clinical ... stents, balloons). Collaborate with regulatory bodies and industry partners to validate device performance and predict patient outcomes in a virtual setting. + Stent… more
- Dentsply Sirona (Waltham, MA)
- …Experience: + 5(+) years of experience in regulatory affairs, preferably in the medical device industry. + Experience with leading regulatory submissions and ... EU technical files submissions. + Provides regulatory guidance and support to cross-functional teams throughout the product lifecycle. Reviews...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 ... for US, EU (EU MDR), and other international geographies. + Experience with medical device software requirements and software regulations. + Ability to identify… more
- Baylor Scott & White Health (Grapevine, TX)
- …BLS within 30 days of hire/transfer. + ARRT-R Radiography (ARRT-R), Cert Cardiac Device Spec (CCDS), Cert EP Specialist (CEPS), Medical Radiologic Tech (MRT), ... **Baylor Regional Medical Center Grapevine Address: 1650 W College St,...and intervention, thrombectomy, EP- Ablation (afib, flutter, SVT, VOM), device placement (pacemaker, defibrillator, CCM, loop recorder). **On-Call:** STEMI… more
- BD (Becton, Dickinson and Company) (Tempe, AZ)
- …possible** with us. **Job Responsibilities:** + Technical leadership skills including familiarity with medical device operations (eg, medical device ... years' experience in engineering or Quality engineering experience within the medical device , pharmaceutical, or equivalent industry **Knowledge and Skills**… more
- Actalent (Anoka, MN)
- …estimation. + Support and comply with company Quality System, ISO, and medical device requirements. + Read, understand, and follow work instructions and ... assembly, and molding. You will also provide direction and support for existing products to optimize processes and ensure...in a machine shop environment. + Experience in the medical device industry. + Expertise in process/continuous… more