...other medical fields by monitoring a variety of chronic conditions, ultimately improving the health and quality of life for patients around the world. The company's innovative solutions provide compre...
...other MotherDuck engineers and our users.Collaborate with frontend and platform engineering teams to ensure our product functions seamlessly.Optimize database performance, network throughput, and reli...
We are looking for enthusiastic starting, junior and medior engineers with an interest for everything that is Life Sciences (Pharmaceuticals, Biotechnology, Medical Devices, Safety & Health). As a pro...
...medical device industry with significant class 2 medical device experience demonstrating progressive leadership, and experience with software as a medical device (SAMD), software as a service (SaaS), ...
.../NL. To perform the operational quality-related tasks in SA/NL and EMEA. To provide in-depth knowledge and support for Quality Systems (VQD / Trackwise / LM Success Factors) To participate on regional...
...Medical Development regulations as in FDA 21 CFR part 820, ISO 13485, ISO 14791, The Medical Device Directive, Safety as in EN60601-1 and EMC as in EN60601-1-2 and subordinate regulations.About Philip...
.../ solutions to support the R&D organization to deliver high quality code, faster. Define and drive our R&D Development build infrastructure architecture. You are key stakeholder in the SW architecture...
...otherwise we arrange an appointment for you) 5. Your VCA-certificate. VCA Basic Safety English (B-VCA) (Only when you have one) Shared cooking facilities / bathroom /WIFI Registration at a Dutch healt...
.../ solutions to support the R&D organization to deliver high quality code, faster. Define and drive our R&D Development build infrastructure architecture. You are key stakeholder in the SW architecture...
...Medical Devices or other safety-critical areas (automotive, aviation, military). Plus: you worked with usability standards specific to medical devices (IEC 62366, FDA guidance, EU-MDR, and CMDE). And ...
...medical.comor +31 (0)33 7548713. Not the right job for you? Take a look at our other vacancies and follow us onLinkedIn.#J-18808-Ljbffr
...Medical Development regulations as in FDA 21 CFR part 820, ISO 13485, ISO 14791, The Medical Device Directive, Safety as in EN60601-1 and EMC as in EN60601-1-2 and subordinate regulations.About Philip...
.../her/hers, he/her/his, they/them/theirs, etc.).#J-18808-Ljbffr
...other Sub-teams (e.g., Study Management, Clinical,) Proactively identify regulatory or related risks/issues and develops mitigation and/or contingency plan. Oversee and guide the preparation, compilat...
...medical device) and/or experience working in a bio-hazard/lab environment preferred. Experience creating and analyzing charts and Pareto charts in MS Excel a plus. Experience or certification in Lean ...