- Hologic (Marlborough, MA)
- …,** leading major US and global clinical trials across multiple phases of medical device development. You'll ensure studies are executed on-time, on-budget, and ... Clinical Project Manager 4 United States Newark, DE, United States...academic-industrial partnerships and with sponsors or CROs in the medical device industry. + Proven track record… more
- ZOLL Medical Corporation (Chelmsford, MA)
- …contract negotiation, and cost management experience required + Consulting or Medical Device industry experience preferred Knowledge, Skills and Abilities ... that make a meaningful difference in people's lives. Our medical devices, software and related services are used worldwide...impact the Key Metrics like OTD, Cost Savings, and Quality . Perform Spend Analysis and rationalization to build and… more
- ConvaTec (Lexington, MA)
- …to 10 years of clinical trial management experience in conducting and leading global medical device clinical trials, preferably with a sponsor company. + Solid ... **About Convatec** **Pioneering trusted medical solutions to improve the lives we touch:**...learn more please visit http://www.convatecgroup.com **Position Overview:** The Sr. Manager , Clinical Operations plays a key role to the… more
- Teradyne (North Reading, MA)
- …Test Equipment (ATE) industry. This key management role requires a hands-on technical manager to lead a Software quality engineering team of 6-8 software ... powering next-generation technologies through sophisticated solutions. Behind every electronic device you use, Teradyne's test technology ensures your device… more
- Hologic (Marlborough, MA)
- …strategies to ensure compliance with QMS standards. + Own compliance strategy for the medical device portfolio, including standards like IEC 60601. + Manage and ... Capital Sustaining R&D Manager Marlborough, MA, United States Join Hologic's Surgical...Biomedical Engineering. + 8+ years of experience in the medical device industry, preferably sustaining complex capital… more
- Olympus Corporation of the Americas (Westborough, MA)
- …matter expertise, technical guidance, and leadership for the application of health and medical device SW regulatory standards to the Olympus SDLC, including IEC ... **Job Description** This role provides professional expertise for Software quality and best practices in SW design, development, release,...+ Minimum of 6 years of experience in a medical device setting. + Experience in the… more
- Medtronic (Boston, MA)
- …multiple teams to execute concurrent, interdependent projects. + Knowledge of medical device R&D, product development, and clinical/regulatory procedures; ... charge in ensuring customer satisfaction design integrity, and impeccable quality across each milestone. Join our esteemed team as...as a Subject Matter Expert + Comprehensive knowledge of medical device standards and regulations (eg, IEC… more
- Stryker (Boston, MA)
- …health data partners to identifyadditionalreal-world data sources for medical device evidence generation. + Ensure quality and performance standards for ... As a **Program Manager , Real-World Evidence** oversees and manages the design...observationalresearch in academia, a contract research organization, or the medical device or pharmaceutical industry + Hands-on… more
- Philips (Cambridge, MA)
- …the right fit if:** + You have a minimum of 10+ years' combined experience in Medical Device Clinical Research and Medical Device development within FDA ... management, and improvement initiatives. + Assists in the updates and enhancement of quality system processes for Clinical & Medical Affairs, aligning with… more
- Dentsply Sirona (Waltham, MA)
- …Experience: + 5(+) years of experience in regulatory affairs, preferably in the medical device industry. + Experience with leading regulatory submissions and ... of world class brands. Dentsply Sirona's products provide innovative, high- quality and effective solutions to advance patient care and...13485, EU MDR). + Experience with software as a medical device , AI and/or medical … more