- Amgen (Cambridge, MA)
- …automate model creation and post/processing. + Experience with combination products and device regulatory requirements, medical device development and design ... do this. Let's change the world. In this vital role you will apply engineering principles to develop efficient and trustworthy models addressing a wide variety of… more
- Fresenius Medical Center (Lawrence, MA)
- …alignment across the organization. + Provide planning and project management support for medical device product launches. + Assist in the development and ... process with Research and Development by applying human factors engineering principles to optimize usability, cost, quality ,...years of experience as a Product Manager in a medical device field or (ii) Master's degree… more
- Medtronic (Boston, MA)
- …plays a critical role in ensuring the security of Medtronic Surgical Operating Unit medical device solutions. Reporting to the Director of Product Security, this ... our security posture. **Careers that Change Lives** In this engineering -focused role, you will join a world-class team of...impact by exploring a career with the world's leading Medical Device company, striving "to alleviate pain,… more
- Fresenius Medical Center (Lawrence, MA)
- …accountable for staffing and leading a team of software developers to deliver high quality medical device software. Develop and drive a long-term strategic ... in software development, verification, and standards necessary to meet global medical device regulatory requirements. + Clear understanding of Software… more
- Fresenius Medical Center (Lawrence, MA)
- …geometric tolerance analysis, and documentation is preferred + Strong understanding of medical device development processes + Able to communicate effectively, ... and/or testing of complex electro-mechanical products preferred + Prior medical device experience strongly preferred EO/AA Employer:… more
- Abbott (Burlington, MA)
- …teams; and providing information on product complaints to various teams (eg Regulatory, Quality Engineering ). The other role of the Post Market Surveillance ... types of product complaints. Independently assesses the complaint to determine if a medical device report needs to be filed with various global regulatory… more
- ZOLL Medical Corporation (Chelmsford, MA)
- …area. They possess a deep expertise in Python, CI/CD integration, and quality engineering across the software development lifecycle.Essential Functions + ... frameworks and tools to verify the software within a software-driven electro-mechanical medical device + Design, develop, and support automated unit,… 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
- Globus Medical, Inc. (Methuen, MA)
- …with cross-functional teams-including systems, electrical, software, manufacturing, and quality engineering -to drive innovative, reliable, and high-performance ... sense of urgency to deliver innovations that improve the quality of life of patients with musculoskeletal disorders. Our...prints using GD&T and tolerance analysis + Experience in Medical Device field **Physical Demands** **:** The… more
- Medtronic (Boston, MA)
- …**Nice to Have (Preferred Qualifications):** + Experience at Medtronic or within the medical device industry + Experience in the management of clinical devices. ... of existing devices; serving as a technical resource between engineering , clinical research, and the medical community....for all ablation procedures at study sites for investigational device studies to guide the physician on the requirements… more