- Cretex (Brooklyn Park, MN)
- …standards, documentation, and integration practices. + Support and comply with company Quality System, ISO 13485, and medical - device regulatory requirements. ... is a leading contract manufacturer of precision components and assemblies for the medical device industry. Our customers view us as a trusted partner in… more
- Medtronic (Minneapolis, MN)
- …the following tasks: + Product Security - Implement security requirements across the medical device development lifecycle by collaborating with teams to uphold ... the patients and sensitive data. The Sr. Product Security Engineer will be acting at this frontline of these...and the use of Hardware Security Modules (HSMs) for medical device protection. + Use of advanced… more
- Insight Global (Eagan, MN)
- …Description We are seeking a Senior Design Engineer to join a medical device manufacturing company's Research, Development & Engineering (RD&E) team. This is ... a high-impact role for a creative, high-energy engineer who thrives on innovation and autonomy. As the...create models, drawings, and layouts. - Ensure compliance with medical device regulations and quality … more
- Actalent (Minneapolis, MN)
- Hardware Engineer Job Description Join a dynamic start-up medical device company as a Principal Electrical Engineer . You will be pivotal in supporting ... test protocols and results to meet design control and quality system requirements. + Participate in Design Assurance activities,...data. + Apply engineering knowledge and knowledge of the medical device industry to assist in developing… more
- Fujifilm (St. Paul, MN)
- …+ Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements and all ... **Position Overview** The Senior Upgrade Engineer is responsible for performing upgrades for Fujifilm...for performing upgrades for Fujifilm Healthcare Americas Corporation (HCUS) Medical Informatics (MI) products to all eligible sites. In… more
- Teleflex (Plymouth, MN)
- …is a leading global provider of product development and production services for medical device manufacturers. We set ourselves apart with deep expertise, decades ... Process Development Engineer 2 **Date:** Nov 29, 2025 **Location:** Plymouth,...OEM with technical support and operating knowledge for our medical device operation. This role will conduct… more
- Philips (Plymouth, MN)
- …if:** + You have a minimum of 5+ years' experience in FDA regulated medical device environments, with a focus on Design Assurance/Control, detailed knowledge of ... The Senior Design Assurance Engineer will play a critical role in support...to Design/Process Controls. + You have strong understanding of Medical Device QSR regulations/standards including ISO 13485,… more
- Philips (Plymouth, MN)
- …8+ years of experience in Software Quality and/or Software Development in medical device industry with hands on experience with SW Design verification and/or ... **Sr. Software Design Assurance Engineer ** **In this role you** Will support New...Management for medical devices and IEC 62304 Medical Device Software. + Serving as SME… more
- Medtronic (Mounds View, MN)
- …PhD with 0 years of relevant experience **Preferred Qualifications** + Knowledge of Medical device software development, IEC-62304 and FDA guidance in a ... of professional growth and cross-functional collaboration as we work together to engineer the extraordinary. Medtronic is seeking a motivated and detail-oriented Sr.… more
- ManpowerGroup (Plymouth, MN)
- Our client, a leading organization in the medical device industry, is seeking a Manufacturing Engineer to join their team. As a Manufacturing Engineer , ... in it for me?** + Opportunity to gain hands-on experience in the medical device industry. + Collaborative work environment supporting professional growth. +… more