- Keeper Security, Inc. (El Dorado Hills, CA)
- …a highly motivated and experienced full stack Senior Software Engineer to join our Support Tools team. The ideal candidate will be a positive and collaborative team ... cybersecurity companies and be responsible for expanding and architecting Keeper's Support Tools! About Keeper Keeper Security is transforming cybersecurity for… more
- IQVIA (Carlsbad, CA)
- _IQVIA has an opportunity with one of the largest medical device manufacturers in the US. We welcome you to apply if interested! You will be asked to create an ... experience by collaborating with healthcare professionals and leading technical initiatives in medical device technology. You will be responsible for leading a… more
- Medtronic (Minneapolis, MN)
- …ICH, IEC). + Proficient understanding of FDA and MDR requirements. + Knowledge of Medical Device Quality Systems (21 CFR 820, ISO 13483) + Experience working ... Effective team member. + Ability to comprehend principles of engineering, physiology, and medical device use. + Good analytical skills. + Ability to effectively… more
- Hologic (San Diego, CA)
- …environment, ideally in the IVD space. + Working knowledge of Quality Management System for Medical Device Manufacturing FDA 21 CFR 820, ISO 13485 as well as CE ... and transfer of Hologic products. + Provide Quality Engineering support for product design and development from...mark requirements, In Vitro Diagnostic Regulation (EU) 2017/746 and Medical Device Regulation (EU) 2017/745, Risk Management… more
- Microsoft Corporation (Redmond, WA)
- …eager to push the boundaries of state-of-the-art graphics systems, engineering systems, and device drivers. Our dynamic and diverse team operates at the cutting edge ... Windows Server ecosystem - through all of these, we support every one of our cloud businesses and billions...feature area. + Creates and implements code for a product , service, or feature, reusing code as applicable. Writes… more
- Astrix Technology (Irvine, CA)
- …our innovative medical devices. You'll lead hands-on investigations, analyze product performance, and support cross-functional improvements - all while ... Knowledge of FDA regulations (21 CFR 820/803), ISO 13485 + Experience with medical device complaint handling and regulatory reporting (MDR, Vigilance, etc.)This… more
- Globus Medical, Inc. (MA)
- …or sales management capacity. + 3-5 years of sales management experience in the medical device industry. + 3-5 years of experience with direct responsibility for ... At Globus Medical , we move with a sense of urgency...amendment process as per assigned accounts. The DCA will support and work closely with Spine Zone Vice Presidents… more
- Medtronic (Brooklyn Center, MN)
- …solving, developing and improving the capability of processes, and navigating the medical device manufacturing quality systems to include regulatory approvals. ... area but is not direct day to day line support Responsibilities may include the following and other duties...experience **Nice to Have:** + Previous experience in the Medical Device Industry + Experience working in… more
- Abbott (Westfield, IN)
- …related discipline + 2-5 years of related experience in Quality + Medical Device experience preferred Apply Now (https://www.jobs.abbott/us/en) * Participants ... highest quality product to the customer. Also provide process/quality engineering support to product development teams, helping to ensure development of… more
- IQVIA (Freehold, NJ)
- …of settings, including but not limited to, the ICU, OR, and Cath Lab. + Ventricular medical device case support , including on call support . + Complete ... part time position will be responsible for providing case support , patient management, and education to both new and...preferred, but not required. + Significant experience with ventricular medical device is required (minimum of 10… more