- 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
- Hologic (Newark, DE)
- Sr. Program Manager , NPD Newark, DE, United States **Senior Program Manager - Medical Device Development** Are you ready to lead groundbreaking programs ... and Expertise:** + Strong familiarity with New Product Introduction (NPI) methodologies, medical device design cycles, and industry standards. + In-depth… more
- Quality Consulting Group (Juncos, PR)
- …in Engineering (preferably) + 5+ years of relevant experience + Experience in medical device design, development & manufacturing. + Experience of products with ... + Proven project execution. + Hands on experience on Projects/Scheduling for Medical Device manufacturing. + Critical thinking and PM skills.(eg project … more
- Teradyne (North Reading, MA)
- …powering next-generation technologies through sophisticated solutions. Behind every electronic device you use, Teradyne's test technology ensures your device ... Teradyne Compute Test Division Engineering team is seeking a hands on first level manager to lead one of our FPGA development teams. Development occurs in a dynamic… 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
- 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
- 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:** Nov 20, 2025 **Location:** Minneapolis,...experience. * Minimum 8 years of clinical research experience, medical device experience preferred. This should includes… more
- Stryker (Mahwah, NJ)
- …experience + Proven new product introduction experience in a regulated industry ( medical device preferred) + Strong knowledge of DFM, process validation, ... As the Advanced Operations & Manufacturing Engineering Manager for New Technology & Product Introduction, you...you will lead a team responsible for transitioning new medical devices from design to full-scale production and sustaining… more
- Medtronic (Jacksonville, FL)
- …initiatives. + Knowledgeable in design, production, and supplier-related efforts for medical device development. + Willingness to travel: 10-25% **Physical ... suppliers to create a sustainable competitive advantage. As part of the GSM Project Management function, the Technical Sourcing Program Manager will lead the… more