- 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
- Medtronic (Minneapolis, MN)
- …in grey area. + Excellent written and verbal communication abilities. + Experience with FDA regulatory medical device requirements, 21CFR Part 806, Part 7; ... overseeing the enterprise FCA planning process, ensuring compliance with quality system requirements, and driving continuous improvement in the...ISO 13485, Medical Device Directive. + Experience supporting internal… more
- GN Hearing (Bloomington, MN)
- …of LEAN methodologies and applying such tools to operations. + Hearing or medical device experience 1-3 years of equipment experience in a production ... Lead and oversee rework efforts, as required. + Perform quality checks on devices. + Identify and drive improvement...ever thought possible. **What We Offer** As a leading medical device manufacturer, we value our employees… more
- Otsuka America Pharmaceutical Inc. (St. Paul, MN)
- …in applying FDA design control requirements (21 CFR ) as applied to medical device software and medical device regulation (IEC-62304) ... commitment to collaborative problem solving, sophisticated design, and the creation of quality products are essential. Your team's primary focus is building core… more
- Medtronic (Fridley, MN)
- …interactive and insightful reports and dashboards using Power BI + Experience in the medical device industry + Experience with 19 Code of Federal Regulations (19 ... with regulatory requirements for US and Canada imports (eg, Customs, FDA , Health Canada, and Participating Government Agencies). Collaborates with 3rd party… more
- Philips (Plymouth, MN)
- …the right fit if:** + You have a minimum of 5+ years' experience in FDA regulated medical device environments, with a focus on Design Assurance/Control, ... the QMS related to Design/Process Controls. + You have strong understanding of Medical Device QSR regulations/standards including ISO 13485, ISO 14971, 21CFR… more
- Abbott (Plymouth, MN)
- …This position works out of our Plymouth MN location in the Structural Heart medical device division. Our business purpose is to restore health and improve ... quality of life by designing and providing ...to maintain regular and predictable attendance **Preferred Qualifications** + Medical device experience preferred, but not required… more
- TE Connectivity (Plymouth, MN)
- … Medical is ranked among the top 10 global companies in the medical device outsourcing industry. The company specializes in the design and manufacture ... across 30 countries, Creganna Medical 's customers include the world's leading medical device and life science companies. Headquartered in Galway, Ireland,… more
- Medtronic (Minneapolis, MN)
- …clinical specialist or a sales/service/engineering position in the Cardiac Rhythm or Implantable Medical Device Industry. Must possess a minimum of two (2) years ... sites, performing activation duties, providing training, encouraging enrollment, ensuring quality data acquisition, and performing study closure activities at… more
- Abbott (St. Paul, MN)
- …for diversity, working mothers, female executives, and scientists. For years, Abbott's medical device businesses have offered technologies that are faster, more ... help people with chronic pain or movement disorders, our medical device technologies are designed to help...help more than 10,000 people have healthier hearts, improve quality of life for thousands of people living with… more