...//lde.tbe.taleo.net/lde01/ats/careers/v2/viewRequisition?org=MSFOCA&cws=53&rid=43428#J-18808-Ljbffr
.../or other regulators, and provides input to establish metrics. Hands on Technical lead: Create analytical solutions for PMS business by combining various data science tools, applied statistics, AI/ML ...
...Medical Image ProcessingJob DescriptionWe’re actively seeking an accomplished AI Engineer with over 5 years of hands-on experience in product development within the realm of medical image processing. ...
.../expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class. Important notice to Employment businesses/ A...
...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...
.../19/2024 Deadline Date:04/30/2024 DescriptionThe Partnership for Supply Chain Management (PFSCM) strengthens, develops, and manages secure, reliable, cost-effective, and sustainable global supply chai...
.../or keen interest in marketplace pricing and inventory. Strong creative problem-solving skills and critical thinking competencies Experience in launching, analyzing, and setting frameworks for A/B tes...