- Edwards Lifesciences (Portland, OR)
- …portfolio of products across TMTT. The Senior Manager will be an experienced medical device professional with strong scientific acumen and a commitment to ... an impact:** + As a key member of the Medical Affairs Clinical Science team, the Senior Manager (formal...PMA applications. + Strong knowledge of scientific research methodology, device development process, GCP, ICH guidelines and Global (US… more
- Medtronic (Jacksonville, FL)
- …ensure seamless integration and compliance. + Develop and review documentation according to medical device regulatory standards (eg, IEC 62304). + Conduct code ... and C++. + Developed and reviewed documentation according to medical device regulatory standards (eg, IEC 62304)....to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference… more
- Edwards Lifesciences (Phoenix, AZ)
- …internal/external working relationships + The Sr. Specialist will be an experienced medical device professional with strong scientific acumen and a commitment ... patients in need. In close partnership with principal investigators, dedicated medical professionals, patient advocacy groups, and regulatory authorities, you will… more
- Medtronic (Juncos, PR)
- …degree with a minimum of 0 years relevant experience. **Nice to Have** + ** Medical Device Development Experience** + Familiarity with FDA regulations (like 21 ... CFR Part 820) or other global medical device standards (ISO 13485, IEC 60601)....to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference… more
- Philips (Plymouth, MN)
- …a Senior Program Manager, you will lead high-impact programs that advance our medical device portfolio, elevate product performance, strengthen product quality & ... that drive product development, lifecycle management, and global execution across multiple medical device portfolios. + Develop and implement program and… more
- ZOLL Medical Corporation (Chelmsford, MA)
- …technical discipline required + At least 5+ years of experience in a medical device or other highly regulated electro-mechanical environment required + ... innovative technologies that make a meaningful difference in people's lives. Our medical devices, software and related services are used worldwide to diagnose and… more
- Stryker (San Jose, CA)
- …Market** to support our Medical 's Digital Health division and portfolio Software as a Medical Device (SaMD)/Software in a Medical Device (SiMD) and ... and Health Hazard Analysis as required in conjunction with R&D and Quality. + Work on process improvement projects...visualization and monitoring. + Exposure to Software as a Medical Device (SaMD), Software in a … more
- Olympus Corporation of the Americas (Westborough, MA)
- …requirements for digital health products and solutions, ensuring compliance with global medical device regulations. As part of a high-growth, innovative team, ... digital health solutions, including Artificial Intelligence (AI) exempt from the medical device classification, and connected technologies. + Provide regulatory… more
- US Tech Solutions (Vernon Hills, IL)
- …in science, math or engineering. Preferred, 1-2 years related experience preferably in medical device or other regulated FDA/QSR and ISO environment. Physical ... Ability to perform testing by following test methods and test protocols from R&D engineers; collecting data and record test results; entering test data into Excel… more
- Cadence Design Systems, Inc. (San Jose, CA)
- …application engineering team for verification to work closely with the best AEs, PEs and R&D in EDA at a company listed in Fortune magazine and Great Place to Work ... this passion into results. By working directly with Cadence R&D and driving customer engagements, you will enhance your...and technical articles - Review new product proposals and device specifications - Assume technical leadership roles in small… more