- US Tech Solutions (San Bruno, CA)
- …with a track record of handling multiple programs and streams of work. + Experience with medical device development standards eg ISO 13485, FDA 21 CFR 820 + ... production and align with Quality System procedures, utilizing expertise in the medical device product development life-cycle, Risk Management,… more
- AbbVie (Pleasanton, CA)
- …(QSR), ISO 13485, ISO 14971, MDR, & MDSAP; + performing all tasks according to medical device development life cycles, manufacturing processes & GMP; & + ... Must have 1 year of quality engineering work experience in FDA regulated medical device manufacturing environment(s). If experience required, must have 1 year… more
- AbbVie (Irvine, CA)
- …LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description AbbVie's Clinical Sciences Development Program - Medical Device consists of three ... audit trends, knowledge management, and robust proactive CAPAs. + Medical Device & Combination Products QA (MDCP...& Combination Products QA (MDCP QA) oversees new product development and risk management activities across a variety of… more
- BD (Becton, Dickinson and Company) (Temecula, CA)
- …experience with a Bachelor's degree + Relevant experience related to combination product or medical device development and/or testing + Ability to work ... performing, and analyzing bench-level engineering tests or research experiments for drug- device combination products and medical devices. The position requires… more
- NVIDIA (Santa Clara, CA)
- …- medical imaging, medical robotics, digital surgery. + Experience with medical device development lifecycle or SaMDs. + Extensive deep learning ... in medical devices and robotics, possesses industry experience in medical device or robotics development , and is enthusiastic about working with… more
- Abbott (Alameda, CA)
- … is required. **Preferred Qualifications** + Solid knowledge of regulations for medical device development , (EN460001, ISO13485, FDA) is desirable. ... preferred + Embedded UI design experience preferred + Detailed experience with medical device development processes and FDA 510K and PMA regulatory… more
- BD (Becton, Dickinson and Company) (Milpitas, CA)
- …other regulatory bodies + Provide subject matter expertise into design of clinical trials for medical device development and submission to the FDA and other ... marketing collateral to support clinical products + Ownership of on-time quality assessments, medical device reporting and health risk assessments to the FDA and… more
- Abbott (Santa Clara, CA)
- …equivalent combination of education and work experience. + Minimum 10 years in medical device development and/or other highly regulated industry. + ... in its creation and the development of this class 3 medical device product in this desirable technology space. Hiring Manager - Lior Noyovitch. **What… more
- Stryker (Irvine, CA)
- …+ Six Sigma Green or Black belts are preferred. + Experience with the medical device development lifecycle, including risk management and design/process ... engineering or related discipline. + 4+ years' related experience required. + Medical device industry experience required. + Familiarity with New Product… more
- ZOLL Medical Corporation (Irvine, CA)
- …a plus + Experience with current unit test frameworks is a plus + Experience with medical device development is helpful but not required ZOLL is a ... innovative technologies that make a meaningful difference in people's lives. Our medical devices, software and related services are used worldwide to diagnose and… more