- NTT America, Inc. (St. Paul, MN)
- …budget. The process is designed to identify and resolve issues early in the design and construction process to ensure quality , reliability, safety, and cost ... and operations teams to understand the project goals and schedule to ensure quality and commissioning activities occur at the appropriate times in the construction… more
- Abbott (Plymouth, 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 heart ... in a regulated environment and clean room experience a plus. Hands-on Medical Device experience preferred. Apply Now (https://www.jobs.abbott/us/en) **Learn more… 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 ... defects. + Communicates issues internally and with suppliers. + Reviews new design specifications and provides input from component quality and manufacturability… more
- Medtronic (Minneapolis, MN)
- …learn, and a problem solver **About Medtronic:** Together, as one of the largest Medical Device companies in the country, we can change healthcare worldwide. At ... to improve lives of millions. Engineering roles in the Quality engineering group can include Quality , Supplier...and conducts technical reliability studies and evaluations of engineering design concepts and design of experiments (DOE)… more
- ManpowerGroup (St. Paul, MN)
- …experience + Strong communication, teamwork, and organizational skills + Experience in medical device industry preferred + Knowledge of risk management, ImV/TMV, ... 2-5 years of experience to support product development and manufacturing quality activities. This role includes risk management, design verification/validation,… more
- Medtronic (Minneapolis, MN)
- …of various government and industry regulations to include FDA QSR 21 CFR 820, EU Medical Device Directive (EU MDD 93/42 EEC), ISO 13485, ISO 9001, and ISO ... controls. Utilize GMP (Good Manufacturing Practices) for Class II and Class III medical devices to ensure quality products and outcomes. Navigate the… more
- Patterson Companies, Inc. (St. Paul, MN)
- …experience with quality management systems and regulatory compliance in the medical device or related regulated field + Developing working knowledge of ... for maintaining and managing the daily operations of the Patterson Quality Management System. Manages compliance activities with responsibility for results in… more
- Danaher Corporation (Chaska, MN)
- …would be a plus if you also possess : + Experience in FDA-regulated or medical device manufacturing environments. + Familiarity with ISO13485, 21 CFR Part 820, ... Miami FL or Brea CA. In this role, you will have the opportunity to: + Design and Implement Scalable Quality Systems Develop and deploy supplier quality … more
- Medtronic (Mounds View, MN)
- …plays a critical role in ensuring the security of Medtronic Surgical Operating Unit medical device solutions. Reporting to the Director of Product Security, this ... and patients. _Make your impact by exploring a career with the world's leading Medical Device company, striving "to alleviate pain, restore health, and extend… more
- Philips (Plymouth, MN)
- …discipline preferred + 5+ years of Supplier Quality Engineering experience in a medical device (Class II & III) or similar environment with manufacturing or ... development through a combination of assessing supplier technical capabilities, supplier quality controls, adherence to design controls, audit, and inspection… more