- Banner Health (MN)
- …team is responsible for the design , build, implementation, and support of medical device integration within a Cerner Oracle environment. The applicant should ... possess a strong understanding of medical device integration with experience in application...knowledge, guidance, research and fact- finding expertise to define, design and modify specifications and processes of complex information… more
- Intertek (Fridley, MN)
- Engineer - Medical Device Electrical Safety, Fridley, MN Interested in future career opportunities in the product testing industry? Intertek, a leading provider ... and Certification) Services, is looking for an Engineer - Medical Device Electrical Safety to join our...and efficiently help clients meet safety, performance, environmental and quality requirements for every market. Spanning a wide range… more
- Capgemini (Minneapolis, MN)
- …+ Perform review of design , development, and testing of software used in medical device product lines. + Actively working to support Automated Test Equipment ... Role - System Test Engineer ( Medical Device ) Location - Minneapolis MN...System Engineers, Hardware and Firmware Engineers. + Ensures the quality of software systems, validate product software requirements, security… more
- Philips (Plymouth, MN)
- **R&D Program Manager - Medical Device NPD (Plymouth, MN)** We are seeking a highly motivated and experienced Program Manager with a background in managing ... experience with a minimum of 7 years in program/project management within the medical device , healthcare, or similarly regulated industry, with proven experience… more
- Philips (Plymouth, MN)
- **Principal Systems Engineer - Medical Device (Plymouth, MN)** In this role, you will contribute to a breakthrough cardiac ultrasound imaging solution that ... You've acquired 10+ years of engineering experience in the design and commercialization of medical products; experience...won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work… more
- Philips (Plymouth, MN)
- …You have a minimum of 8+ years' experience in FDA regulated medical device environments, with a focus on Design Assurance/Control, detailed knowledge of Risk ... The Sr. Manager- Design Assurance Quality Engineering will manage...the creation and review of all medical device documentation including- Safety Classification, Design Verification… more
- Philips (Plymouth, MN)
- …You have a minimum of 5+ years' experience in FDA regulated medical device environments, with a focus on Design Assurance/Control, detailed knowledge of Risk ... as quality system compliance. + Provides critical quality review of design requirement rationales, test...Design /Process Controls. + You have strong understanding of Medical Device QSR regulations/standards including ISO 13485,… more
- ManpowerGroup (Plymouth, MN)
- Manpower Engineering is currently partnering with a twin cities start-up medical device company focused on a novel transcatheter product for heart valve disease ... minimum of four (4) years of experience in class II or class III medical device product development, preferably intravascular devices. + Proven understanding of… more
- Philips (Plymouth, MN)
- …+ You have a minimum of 8+ years' experience in FDA regulated, IEC 62304 medical device software environments (SiMD/SaMD), with a focus on Software Design ... + You have detailed experience in identifying, promoting, and supporting processes and design quality tools for use in tracking/preventing software defects, … more
- Philips (Plymouth, MN)
- …14971, Risk Management for medical devices. + Knowledge of how to apply Design Controls and Process Controls. Provides critical quality review of design ... **Sr. Design Quality Engineer** **In this role...**Sr. Design Quality Engineer** **In this role you** Serve as...**You're the right fit if:** + Good understanding of Medical Device QSR, ISO 13485 and ISO… more