- 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
- 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
- J&J Family of Companies (Danvers, MA)
- …work experience + 2+ years of related experience in Quality Assurance within Medical Device , Diagnostic, Pharmaceutical or other regulated industry + Ability to ... as well as cross functionally with departments such as R&D , Regulatory, Manufacturing, Supplier Quality, and Medical ...Knowledge and application of QSR/GMP/GCP/ISO regulations as related to medical device . + Working knowledge and practical… more
- J&J Family of Companies (Danvers, MA)
- …Biomedical, or related); Master's preferred + 5+ years of experience in medical device engineering, product development, or sustaining engineering + Deep ... technical expertise in cardiovascular or related medical device platforms + Experience supporting regulated product development (FDA, ISO, IEC standards) +… more
- Capgemini (Waltham, MA)
- Role: Software Engineer - C Location: Waltham MA - 100%.... Develop modern C (11' or newer) based standalone medical device applications in Linux OS . ... job you're considering** Join Capgemini as a Senior Software Engineer and make a significant impact in developing innovative...software development, with at least 2 years in the medical device or other regulated industries .… more
- Medtronic (Danvers, MA)
- …(Geometric Dimensioning and Tolerancing), and regulatory requirements. + Experience in a medical device or other highly regulated industry. + Familiarity with ... to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference...We have the talent, diverse perspectives, and guts to engineer the extraordinary. Learn more about our business, mission,… more
- RTX Corporation (Andover, MA)
- …Department, the individual in this role will work as a process development engineer to lead and execute process development efforts, assist in process sustainment, ... improve product yield, develop new processes and device capabilities, and assist in the creation of new...well in small, cross-functional teams, assist in pursuing contract R&D , and assist in transitioning processes into production. +… more
- Capgemini (Boston, MA)
- …impact patient care and clinical outcomes. **Your role** + Design and develop standalone medical device applications using modern C on Linux OS. + Lead the ... job** **you're** **considering** Join Capgemini as aC /MATLAB Software Engineer and help shape the future of healthcare technology....in application software development, with 2 years in the medical device or other regulated industries. +… more
- Hologic (Marlborough, MA)
- …+ In-depth understanding of FDA Quality System Regulations, ISO 13485, and Medical Device Directive. + Expertise in compliance issues and regulatory ... Principal Quality Assurance Engineer Marlborough, MA, United States Louisville, CO, United...and compliance. **Experience:** + Minimum 12+ years in the medical device industry. + Proven track record… more
- Capgemini (Waltham, MA)
- …environment, we'd love to hear from you. **Your role** + Design and develop standalone medical device applications using modern C (C 17 or newer) on Linux OS ... **About the job you're considering** Join Capgemini as an Algorithm Software Engineer and help shape the future of medical innovation. In this onsite role based… more
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