- Abbott (Plymouth, MN)
- …position works out of our Plymouth MN location for our Electrophysiology Medical Device business. In Abbott's Electrophysiology (EP) business, we're advancing ... Ability to travel approximately 10%, including internationally **Preferred Qualifications** Medical device industry experience preferred Masters' degree… more
- Medtronic (Minneapolis, MN)
- …quality engineering/ design assurance engineering. + Familiarity with multiple aspects of medical device quality (eg Design Controls, Supplier Controls, ... managerial experience. **Nice to Have:** + Knowledge of Consumer Electronic and/or Implantable Medical Device Design + DRM Green Belt certification or experience… more
- Abbott (Plymouth, MN)
- …works out of our Plymouth, MN location, supporting our Electrophysiology (EP) medical device division. In Abbott's Electrophysiology (EP) business, we're ... colleagues serve people in more than 160 countries. **Project Manager -Operations New Product Introduction** **Working at Abbott** At...years of experience as an engineer, preferably in the medical device business or other highly regulated… more
- Abbott (Plymouth, MN)
- …requests of senior management. **Required Qualifications** + Prior marketing experience within medical device or healthcare industry. + Bachelors' Degree with 4+ ... Mission: Why We Exist Our business purpose is to restore health and improve quality of life by designing and providing device and management solutions for… more
- Medtronic (MN)
- …to meet deadlines. + Advanced degrees including MS, PhD or MBA. * Specific medical device experience in the electrophysiology field. * Previous clinical support, ... seeking a highly motivated and experienced Global Product and Globalization Program Manager to join our dynamic team. This candidate is responsible for developing… more
- Insight Global (St. Paul, MN)
- …large, complex enterprise-level projects Experience delivering and maintaining systems within a medical device or a highly regulated environment Proven team ... deliver in a challenging, fast paced, rapidly changing environment PMP(R) certification Medical device or regulated industry experience Experience with BSC SAP,… 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 ... The Sr. Manager -Software Design Assurance will play a critical role...performance management, technical/professional development and mentorship to engineers and quality teams, helping them meet schedules, resolve technical challenges,… more
- Olympus Corporation of the Americas (Brooklyn Park, MN)
- …components, and sub-assemblies to ensure compliance with company policies and procedures and medical device regulations. The Product Quality Engineer will ... in Quality Engineering within an FDA regulated medical device manufacturing environment. + Strong working...ability to email, you may call our HR Compliance Manager at 1-888-Olympus (###). **Let's realize your potential, together.**… more
- Medtronic (Brooklyn Center, MN)
- …methods such as laser, resistance, and ultrasonic welding + Knowledge of medical device manufacturing standards, including ISO 13485, FDA regulations, and ... we engineer the extraordinary by transforming bold ideas into life-changing medical technologies. The Medtronic Energy and Component Center (MECC) in Brooklyn… more
- Chemours (St. Paul, MN)
- …Biological Science, Toxicology or comparable technical field + 5+ years of medical device regulatory compliance experience with respect to raw material ... components and/or 5+ years' experience assessing risk associated with materials supplied to medical device customers + Familiarity with US medical device … more