- AbbVie (Cleveland, OH)
- …in compliance with FDA's Quality System Regulation (QSR), ISO13485, the Canadian Medical Device Regulations, and all other international regulatory requirements ... Follow Allergan Aesthetics on LinkedIn. Job Description The Practice Development Manager has general responsibilities for all aspects of customer… more
- Integra LifeSciences (Plainsboro, NJ)
- …corporate policies, US Food and Drug Administration regulations, ISO 9001, ISO 13485, the Medical Device Directive, the Canadian Medical Device ... of quality programs and policies that ensure that the development , manufacture and distribution of medical products...and Drug Administration (FDA) regulations, ISO 9001, ISO 13485:2003, Medical Device Directive (MOD), the Canadian … more
- J&J Family of Companies (Irvine, CA)
- …experience leading Medical /Clinical teams in a regulated, commercial biomedical or medical device business is strongly preferred + Experience in product risk ... ICE Technology, ensuring compliance with regulatory standards and driving innovation in medical technology development . This role will provide strong strategic… more
- ThermoFisher Scientific (San Diego, CA)
- …key business opportunities. Attends and presents sponsor meetings, provides medicines and device development consultation to clients and project team members in ... Coast Region accounts. + In collaboration with the Global Medical Officer, plays leadership role in proposal development...support of sales efforts. + Serves as a regional medical market leader to business development for… more
- Panasonic Avionics Corporation (Irvine, CA)
- …concepts, protocols, and technologies, as well as experience with network stack development , network device drivers, and network interface configuration. + ... is conveniently located in Irvine, CA near John Wayne Airport in the Park Place development . For our onsite and hybrid employees you will be able to enjoy amenities… more
- Stryker (Portage, MI)
- …Assurance** to support our Medical 's Digital Health division and portfolio Software as a Medical Device (SiMD) or Software in a Medical Device (SiMD) ... Digital Health Portfolio, focusing on Acute Care in the Medical Division. + Collaborate on software design, development...+ Experience with regulatory agencies (FDA, MoH, TUV) and medical device regulations (820, IEC 62304/82304, 60601),… more
- ZOLL Medical Corporation (Boston, MA)
- …PhD, or equivalent) is preferred. Experience : + 5+ years of clinical or medical device /pharmaceutical industry experience. Required. + 7+ years of experience in ... presence and reputation. + Collaborate with cross-functional teams, including product development , medical affairs, and marketing, to ensure the integration… more
- Globus Medical, Inc. (Audubon, PA)
- …software engineers to integrate system hardware and firmware into market-ready medical device products** **Evaluate real-world system performance with hands-on ... building, and testing embedded systems, including firmware design and development . This role requires a balance of creative thinking,...in accordance with IEC 60601** **Experience working in the medical device company is a plus** **Excellent… more
- Astrix Technology (Fort Worth, TX)
- …5 years experience OR MS Mechanical Engineering + 3 years experience + 1-2 years medical device experience preferred (Class II/III a plus) + Proficient in Creo ... **Mechanical Engineer I - Medical Devices** Engineering Fort Worth, TX, US Pay...43.50 + Added - 05/09/2025 Apply for Job Exciting development opportunity to work for a global leader dedicated… more
- Edwards Lifesciences (Irvine, CA)
- …* Performing visual, dimensional, and functional inspection across all components and/or finished medical device products using a wide variety of all applicable ... a patient's life. Our Quality teams help shape the development of groundbreaking technologies to ensure each stage of...levels of productivity. * Performing functional testing of finished medical device products using both automated and… more