- Stryker (Irvine, CA)
- …inclusion, and belonging in hiring and team development. + Ensure compliance with medical device regulations and design control standards. + Partner with ... by a mission to make healthcare better. As a ** Manager ,** **R&D Engineering - New Product Development (NPD)** ,...deliver complex projects. + Experience with regulatory compliance in medical device development. + Proficiency in CAD… more
- J&J Family of Companies (West Chester, PA)
- …+ Minimum of 5 years of program management experience or equivalent in the medical device or similar highly regulated industry + Proficiency in Microsoft ... impact health for humanity. Learn more at https://www.jnj.com **Job Function:** Project /Program Management Group **Job Sub** **Function:** R&D Project Management… more
- Abbott (Alameda, CA)
- …customer service and program development within a highly regulated environment, ideally in medical device or similar regulated industry. + **Minimum 2 years of ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more
- Hologic (Newark, DE)
- Sr. Program Manager , NPD Newark, DE, United States United States **Senior Program Manager - Medical Device Development** Are you ready to lead ... and Expertise:** + Strong familiarity with New Product Introduction (NPI) methodologies, medical device design cycles, and industry standards. + In-depth… more
- Medtronic (Boston, MA)
- …best practices, test automation strategies, and emerging technologies relevant to medical device software. + Champion and implement Lean-Scaled Agile ... + Ensure all software verification activities adhere to relevant medical device regulations (eg, FDA 21 CFR...components. + Participate in design reviews, risk assessments, and project planning to provide early feedback on software design… more
- Edwards Lifesciences (Salt Lake City, UT)
- …ensures operational excellence, technology readiness, capacity planning, and compliance with medical device quality and safety requirements while serving ... calibration systems, process controls, and traceability appropriate for regulated medical device manufacturing. + Drive process optimization through… more
- Teleflex (Houston, TX)
- …clinical exposure in the medical field in the Cardiology environment. * Medical Device industry supporting Clinical and Medical Affairs, strongly ... Clinical Affairs Manager , Interventional Access (REMOTE) **Date:** Dec 8, 2025...with FDA's Quality System Regulation (QSR), ISO13485, the Canadian Medical Device Regulations, and all other international… more
- Medtronic (San Diego, CA)
- …+ Proven ability to influence and negotiate internally and with customers. + Medical device product/industry/technical acumen + Proven ability to work globally + ... Diabetes organization is looking for a Software Technical Program Manager to join our Software Operations Organization to in...aspects of ongoing projects and serves as liaison between project management and planning, project team, and… more
- Teleflex (Minneapolis, MN)
- …ability to be detail-oriented, organized, and productive with a keen interest in medical device and biologics research. **Principal Responsibilities** * Manage a ... Clinical Research Associate Manager (REMOTE) **Date:** Dec 19, 2025 **Location:** Minneapolis,...experience. * Minimum 8 years of clinical research experience, medical device experience preferred. This should includes… more
- Olympus Corporation of the Americas (Center Valley, PA)
- …of 6 years of experience. + Prior experience in a sponsor, CRO, or medical device company. In-depth knowledge and experience with FDA regulations and familiarity ... and GCDMP. + Strong expertise in implementing and maintaining systems for global medical device trials (Class II/III or combination products). + Excellent… more