- Globus Medical, Inc. (San Diego, CA)
- …+ Minimum five years of mechanical design engineering experience, preferably in the medical device field + Bachelor's degree in Mechanical Engineering or similar ... At Globus Medical , we move with a sense of urgency...compliance with Globus quality system and other applicable regulatory bodies + Design and develop instruments and implants… more
- Abbott (Santa Clara, CA)
- …meet the existing and emerging regulatory requirements, particularly the EU Medical Device Regulations (EU MDR) and ISO 10993 series. **Principal ... Biocompatibility support to the research & development of new medical device products as well as the...devices and related documentation to ensure biocompatibility and appropriate Regulatory and Quality compliance . + Oversee development… more
- Gilead Sciences, Inc. (Foster City, CA)
- …communication skills are required. + Demonstrated ability to facilitate the interface with medical device vendors and HF consulting firms. + Demonstrated ability ... including realistic timeline estimates for HFE activities. + A deepknowledge of the regulatory and compliance requirements for HFE and combination product risk… more
- Abbott (Sylmar, CA)
- …spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues ... you dream of + Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO...business objectives and patient outcome metrics. + Collaborate with device engineering, software, and digital teams to embed AI… more
- Medtronic (Northridge, CA)
- …framework, ensuring compliance with ISO 10993 standards and global medical device regulations. This role involves conducting comprehensive biocompatibility ... related fields. MS or PhD preferred. + Strong understanding of ISO 10993 and global medical device regulations (eg, EU MDR, FDA, REACH, Prop 65). + Experience… more
- J&J Family of Companies (Santa Clara, CA)
- …design and development. **Essential Job Functions** + Lead the software development for medical device product(s) in full compliance with the company's ... Medical portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated… more
- Veterans Affairs, Veterans Health Administration (Long Beach, CA)
- …limited oversight by senior biomedical engineers. They participate in medical device hazard investigations, to assure compliance with patient safety goals, ... and safety alert program for medical devices, including medical device hazard investigations, to assure compliance with patient safety goals, SMDA, and… 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 ... 10+ years of experience in advanced analytics, AI, or data science within the medical device , medtech, or pharmaceutical industry. + Strong expertise in machine… 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 ... concept through transfer to PDP team. + Design and develop product(s) in compliance with the company's Design Control requirements and consistent with applicable … more
- Globus Medical, Inc. (Redwood City, CA)
- …3 years with a PhD - related experience with development or verification in the medical device industry. (class III medical device experience preferred). ... At Globus Medical , we move with a sense of urgency...and validation plans and reports. Works with Quality and Regulatory Engineers for the release and submission of technical… more
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