- Stryker (Minnetonka, MN)
- …Fri, 8am - 5pm** + Overtime based on business needs **What you will do** As a Senior Medical Device Driver, you will be responsible for the distribution and ... below any applicable local minimum wage rates. Health benefits include: Medical and prescription drug insurance, dental insurance, vision insurance, critical illness… more
- Fujifilm (St. Paul, MN)
- …to be an integral part of the legal team providing support to the Medical Device businesses of FUJIFILM Healthcare Americas Corporation and FUJIFILM SonoSite, ... responsible for working independently and collaboratively on legal issues affecting the Medical Device businesses to minimize risks of legal liability and… more
- Oracle (St. Paul, MN)
- …for CE marking processes and requirements under the EU Medical Device Regulation (EU MDR). **Responsibilities** The Senior Compliance Manager will provide ... file development and maintenance, risk management, and post-market surveillance for medical device market access. The Senior Compliance Manager coordinates… more
- LCI-Lawinger Consulting (Fridley, MN)
- …Manager is responsible for planning, managing, and executing complex, multi- device product development projects in alignment with applicable standard operating ... field; 15+ years of experience in a regulated industry (eg, pharmaceuticals or medical devices). + Minimum 10 years of project management experience in a regulated… more
- ManpowerGroup (St. Paul, MN)
- We are partnering with a medical device manufacturer to hire a ** Senior Process Development Engineer** who will provide technical leadership in the ... Engineering, or related field + 6+ years of engineering experience in the medical device industry + Strong background in process development, validation, and… more
- Danaher Corporation (Minneapolis, MN)
- …years' experience in Project Management . + Significant experience in medical device /diagnostics regulated environment (manufacturing, R&D, supply chain, ... design changes, and all aspects of technology transfer programs/projects in the Medical Device or Diagnostics regulatory environment + Excellent leadership,… more
- Abbott (Maple Grove, 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...Paul, MN currently has an on-site opportunity for a ** Senior Medical Writer, Clinical Evaluation** . The… more
- Edwards Lifesciences (Minneapolis, MN)
- …of products across TMTT. The Senior Manager will be an experienced medical device professional with strong scientific acumen and a commitment to putting ... an impact:** + As a key member of the Medical Affairs Clinical Science team, the Senior ...PMA applications. + Strong knowledge of scientific research methodology, device development process, GCP, ICH guidelines and Global (US… more
- Abbott (Plymouth, MN)
- …help of international regulatory affiliates. + Compile, prepare, review and submit medical device submissions to regulatory agencies + Interfaces directly with ... ongoing surveillance and analysis of all pertinent domestic and international medical device regulations to ensure submission requirements world-wide are… 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 performing upgrades for Fujifilm Healthcare Americas Corporation (HCUS) Medical Informatics (MI) products to all eligible sites. In… more