- Abbott (Sylmar, CA)
- …supporting projects/programs in terms of biocompatibility of medical devices , materials, and processes. The manager will represent our business unit(s) ... ISO 10993. Additionally, this role requires knowledge of the medical device biocompatibility discipline throughout...appropriate to product development and change activities for assigned devices . The Biocompatibility Manager must… more
- J&J Family of Companies (Santa Clara, CA)
- …Medical portfolio aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated ... Johnson & Johnson is hiring for a **Quality Engineer Manager ** **- Shockwave Medica** l to join our team...in an engineering discipline with 10 years' experience in Medical Device Quality, Manufacturing, or Engineering including… more
- TE Connectivity (Wilsonville, OR)
- … tubing, including heat shrink and extruded components, used in advanced medical devices and interventional therapies. This role combines hands-on technical ... or related discipline. + Minimum 7+ years of experience in product development of medical device components, with a focus on polymer extrusion and heat shrink… more
- AbbVie (Pleasanton, CA)
- …successful execution of the Design Control Process for complex electromechanical medical devices containing hardware, software, electrical and mechanical ... experience as a quality engineer or closely related role within a medical device environment. Alternatively, Employer will accept alternate combination of… more
- GE HealthCare (Chicago, IL)
- …minimum of 6 years combined work experience in heavily regulated fields such as medical devices , pharmaceuticals, or biologics. + A minimum of 5 years' ... + Experience with Software (SiMD or SaMD), cybersecurity, and other non- device software products. + Experience with Biocompatibility standards and… more
- Medtronic (North Haven, CT)
- …standards such as ISO 17664, ANSI/AAMI ST98, ISO 15883-5, and European medical device regulations, to support the regulatory submission of implantable ... cleaning cycle development strategies for a variety of reusable medical devices including Class II and/or III...to ISO 17664, ANSI/AAMI ST98, ISO 15883-5, and European medical device regulations and standards. + Assists… more