with FDA, ISO 13485, IEC 60601, or other relevant medical device standards. Experience with low-power design and miniaturized... to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every...
IEC 60601 Experience with reliability testing Demonstrated use of Quality tools/methodologies Strong written/verbal... Previous R&D experience Strong knowledge of QSR and ISO standards Medical device experience ASQ certification Requisition...
, and suppliers. Mentor engineers and leaders across R&D, New Product Development, and Operations to build and maintain a robust.... Proficiency in 21 CFR Part 820, ISO 13485, ISO 14971, IEC 62304, IEC 60601, IEC 62366, ISO 27001, and EU MDR compliance frameworks...
and is also a certified CAR-T center for Novartis, Kite and BMS. FACT Accredited and Immune Effector Cell (IEC) program that performs... time Job Requisition ID: R-47878 We are an equal employment opportunity employer without regard to a person’s race...
in healthcare systems. About Sanofi: We’re an R&D-driven, AI-powered biopharma company committed to improving people’s lives..., or MBA 5+ years of experience in design controls and FDA / ISO 13485 / IEC 62304 compliant software development, regulatory...
and/or standards knowledge to be considered a domain expert (SME) that can be assigned and work independently on long lead R&D projects... status and test results to R&D client, sales personnel, and management throughout testing. Provide ongoing support...
of all performed procedures in assisting in implementation of ISO / IEC 17025:2005 in the laboratory Maintain the good laboratory... that their products, materials, processes and services are safe, compliant and fit for purpose. From early R&D, through complex regulatory...
of all performed procedures in assisting in implementation of ISO / IEC 17025:2005 in the laboratory Maintain the good laboratory... that their products, materials, processes and services are safe, compliant and fit for purpose. From early R&D, through complex regulatory...
about improving patient outcomes across our increasing and wide range of complex systems-based products. As part of the R&D team..., MA office at least three days per week. Your responsibilities will include: Act as an R&D Technical Lead responsible...
about improving patient outcomes across our increasing and wide range of complex systems-based products. As part of the R&D team..., MA office at least three days per week. Your responsibilities will include: Act as an R&D Technical Lead responsible...