- Meta (Burlingame, CA)
- …relevant technical field, or equivalent practical experience 7. 5+ years of experience in medical device system engineering or a related role 8. ... Verification and Validation Engineer to join our medical devices compliance team, focusing on wearables...compliance team, focusing on wearables and Software as a Medical Device (SaMD). This role will be… more
- Capgemini (Burlington, MA)
- …manage a team of engineers, and ensure compliance with medical device regulations. **Your Role** . Lead Verification Strategy: Develop and execute ... Ensure all verification activities align with relevant medical device regulations such as ISO 13485,...of cybersecurity and data privacy in medical systems . . Familiarity with medical device… more
- ZOLL Medical Corporation (Broomfield, CO)
- …provide innovative technologies that make a meaningful difference in people's lives. Our medical devices , software and related services are used worldwide to ... and treat patients suffering from serious cardiopulmonary and respiratory conditions.ZOLL Data Systems , a division of ZOLL Medical Corporation, is a healthcare… more
- ZOLL Medical Corporation (Pittsburgh, PA)
- …provide innovative technologies that make a meaningful difference in people's lives. Our medical devices , software and related services are used worldwide to ... death. + HFMS (https://cardiacdiagnostics.zoll.com/products/heart-failure-arrhythmia-management- system /) (Heart Failure Management system ) is a non-invasive, patch-based device that… more
- Lilly (Indianapolis, IN)
- …for the purpose of crafting, developing, launching, and continuously improving proprietary delivery device systems . This business is unique to the broader Lilly ... allocation + Create and manage traceability from requirements (including system risk) to system verification /validation...Engineering in a regulated industry, or experience working on medical devices + 2+ years of work… more
- Wolters Kluwer (Indianapolis, IN)
- …portfolio of on-market medical devices including Software as a Medical Device (SaMD) within the Health Division in Wolters Kluwer. Important ... regulations, 510(k)s, labeling and promotional materials, 21 CFR 820, global medical device registration, technical writing, and external standards.… more
- US Tech Solutions (San Bruno, CA)
- …align with Quality System procedures, utilizing expertise in the medical device product development life-cycle, Risk Management, Design/Process ... audit readiness and regulatory submissions. + Support bringing novel medical devices from concept to release, manage... Manufacturing or Software as a Medical Device (SaMD). + Experience with Quality Management Systems… more
- Merck (Rahway, NJ)
- …benchtop/low-volume to high-volume clinical and commercial assembly equipment and processes for medical devices /drug delivery systems . Reporting to the ... to develop robust assembly specifications with sound justification. + Understand medical device /delivery system product design, functionality, storage,… more
- Takeda Pharmaceuticals (Lexington, MA)
- …+ Develop Device Clinical Development Strategy for Combination Products and Medical Devices + Develop comprehensive risk management strategies for devices ... device , or pharmaceutical industry experience + Experience with both medical devices , drug- device combination products, digital health technologies… more
- Merck (Rahway, NJ)
- …The ideal candidate will possess extensive knowledge in medical device engineering, particularly in the design, manufacturing, verification , validation and ... of product and process development in the (bio)pharmaceutical and medical device industries to set tactical and...subject-matter experts within the broader DD&T team (eg design verification , device risk management, human factors, technical… more
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