- HonorHealth (AZ)
- …maintenance, electrical safety inspections, and quality assurance consistent with applicable regulatory standards on assigned medical equipment in a timely ... area. The comprehensive network encompasses six acute-care hospitals, an extensive medical group with primary, specialty and urgent care services, a cancer… more
- Fujifilm (Boston, MA)
- …+ Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements ... with Key Accounts and Opinion Leaders within the Liver/Hepatology Medical Oncology community. Manage specific assigned geographic areas and successfully… more
- Globus Medical, Inc. (Audubon, PA)
- …required + Minimum of 2 years of progressive work experience, preferably in the medical device industry or other regulated industry + Ability to review ... be to manage and organize all Quality Documentation that is required by Globus Medical Inc and other regulatory agencies. This will include issuing, maintaining,… more
- Penn Medicine (Philadelphia, PA)
- …(CE) team, providing Clinical Engineering guidance around the implementation of medical devices and managing our Medical Device Cyber Security program. ... of healthcare. That involves interacting with clinicians, educators, networking, MDS (interfacing medical devices with other systems), regulatory , safety,… more
- Abbott (Lake Forest, IL)
- …the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000 ... development, validation, and security practices. Collaborate cross-functionally to secure medical device and non- medical ...development and validation, with 5+ years in cybersecurity for medical devices . + Proven expertise in regulated… more
- J&J Family of Companies (Santa Clara, CA)
- …Medical portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated ... and tooling for multi- and single-lumen tubing used in medical devices . Under minimal supervision, the Principal...relevant engineering degree and 10 years' experience in the medical device industry or a Master's Degree… more
- General Motors (Warren, MI)
- …against industrial safety standards (ISO 13849, ISO 61508) or in an analogous regulatory environment (eg medical devices ) + Exposure to manufacturing ... environments and previous experience fielding products into live production This job may be eligible for relocation benefits. **About GM** Our vision is a world with Zero Crashes, Zero Emissions and Zero Congestion and we embrace the responsibility to lead the… more
- Wolters Kluwer (Juneau, AK)
- …and other software tools to for-profit corporations including CROs, pharma and medical device companies. The **Senior Account & Relationship Manager** will ... calling primarily on Librarians, Information Scientists, Heads of Global Regulatory Affairs, Directors of Medical Affairs, and...+ Proven track record selling into the pharmaceutical and medical device companies, and CRO's (preferred) +… more
- Terumo Medical Corporation (Elkton, MD)
- …business goals and regulatory compliance in the design and manufacture of medical devices within the Manufacturing and Distribution Locations at TMC. This ... manufactures, and markets a complete, solutions-based portfolio of high-quality medical devices used in a broad range...Device History Records (eDHR) meet quality standards and regulatory guidelines. 7. Lead the design and implementation of… more
- Medtronic (Milwaukee, WI)
- …studies for cost control, waste reduction and inventory control; NC & CAPA Investigations; Medical Device Quality & Regulatory Compliance (FDA 21 CFR Part ... development of Class I, Class II and Class III Medical Devices by supporting machining, packaging, warehousing,...years' experience with each of the following: Manufacturing in medical device industry including Class I, Class… more