- ManpowerGroup (Minneapolis, MN)
- …(NO REMOTE CANDIDATES)** **12+ month contract** **Summary** : Software developed for the medical device industry requires rigor and attention to detail to meet ... is in tune with the highly regulated nature of medical device software. We're looking for a...for a top-notch software engineer with a focus on quality who has experience with iOS development (Swift). **Key… more
- Danaher Corporation (Chaska, MN)
- …manage medium/large design changes and technology transfer projects in the Medical Device or Diagnostics regulatory environment, ensuring compliance with ISO ... experience leading multiple projects/a project manager + Prior experience in Medical Device manufacturing environments + Change Management Certification desired… more
- Bausch + Lomb (St. Paul, MN)
- …R&D/Project Management, Clinical/ Medical Affairs, Biometrics, Regulatory Affairs, Quality Assurance, Pharmacovigilance/GPSS and Drug/ Device Safety, and ... provide input on study-related documents and issues (DMP, SAP, drug/ device supplies, CSR, etc.). + Provides clinical operations input...ICH, GCP and B&L SOPs. + Responsible for the quality of all study-related documentation (eg, Trial Master File,… more
- Abbott (St. Paul, MN)
- …Product Development to ensure Design for Manufacturability in the electromechanical medical device space. + Analyze and solve problems from basic engineering ... work experience. + Minimum 5 years manufacturing engineering experience. Medical device experience required. International manufacturing experience preferred.… more
- Philips (Plymouth, MN)
- …responsible for interpreting complex engineering requirements to devise and deliver optimal design solutions for sophisticated medical device components, ... role:** + Interprets complex engineering requirements to devise and deliver optimal design solutions for sophisticated medical device components,… more
- Medtronic (Mounds View, MN)
- …complying with government regulations. + Evaluate incoming information to determine Medical Device Reporting and Vigilance reporting eligibility. + Ensure ... complete, accurate, and timely submission of Medical Device Reports (MDRs), Vigilance Reports (VR)...Previous Medtronic work experience + Experience in a customer quality experience management function + Degree in Health Care,… more
- Medtronic (Mounds View, MN)
- …of 8years of relevant experience **Preferred Qualifications** + Extensive experience in medical device or highly regulated industries. + Expertise in designing, ... will work cross-functionally with teams in mechanical engineering, software development, quality assurance, and manufacturing to drive projects from concept through… more
- Abbott (St. Paul, MN)
- …purpose is to restore health and improve quality of life through the design and provision of device and management solutions for the treatment of structural ... decisions and judgments with minimal supervision **Preferred Qualifications** + Previous medical device , manufacturing or assembly experience is helpful **Learn… more
- Abbott (St. Paul, MN)
- …purpose is to restore health and improve quality of life through the design and provision of device and management solutions for the treatment of structural ... both written and oral form + Participate in continuous improvement/ quality initiatives in order to enhance production processes to...necessary to perform at this level, preferably in the medical device industry. + Incumbents are required… more
- Medtronic (Mounds View, MN)
- …promotional materials Must Have: Minimum Requirements Bachelors degree with 7+ years of medical device regulatory affairs experience OR An advanced degree with ... for R&D, QA, Operations, functional COEs, regional Regulatory and Quality , and the Medtronic Enterprise Focuses on tactical, operational...5+ years of medical device regulatory affairs experience Nice to… more