- WSP USA (Minneapolis, MN)
- …grounding touch and step potentials, short circuit study, protective device coordination, one-line diagram development, protective relaying, and substation ... work conforms with specifications, permit applications, compliance documentation, and regulatory and technical analysis memos. + Prepare data and visualizations… 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 ... of the business, to work on customer systems. + Adheres to the Company's quality and regulatory compliance requirements, without exception, and ensures that all… more
- Medtronic (Mounds View, MN)
- …of 8years of relevant experience **Preferred Qualifications** + Extensive experience in medical device or highly regulated industries. + Expertise in designing, ... to the design, development, and testing of electrical systems and circuits for medical devices, ensuring compliance with applicable regulatory standards (eg, IEC… more
- Danaher Corporation (Chaska, MN)
- …also possess previous experience in: + Experience in the FDA-regulated diagnostics or medical device industry. + Exposure to the Danaher Business System (DBS) ... development of enterprise AI and automation solutions that enhance workflows across Quality , Regulatory , and Clinical Affairs (QRC). This role blends project… more
- Danaher Corporation (Chaska, MN)
- …lifecycle management within the Diagnostics industry or a related field (eg, Medical Device , Pharmaceuticals, Biotechnology, Life Sciences) and a deep knowledge ... Managers towards it; build and maintain strong relationships with R&D, Clinical & Regulatory Affairs, Marketing, Operations, and Quality + Own & improve Beckman… more
- Abbott (Plymouth, MN)
- …to detail. + Ability to maintain regular and predictable attendance. + Experience in Medical Device or similar field preferred. **Learn more about our health and ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… 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 ... of the business, to work on customer systems. + Adheres to the Company's quality and regulatory compliance requirements, without exception, and ensures that all… 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 or post go-live support cases in compliance with the company's quality procedures. **Company Overview** At FUJIFILM Healthcare Americas Corporation, we're on a… more
- Edwards Lifesciences (Minneapolis, MN)
- …assigned studies + Contributing to additional initiatives that shape the future of medical device development **What you'll need (Required):** + Ph.D. or ... patients in need. In close partnership with principal investigators, dedicated medical professionals, patient advocacy groups, and regulatory authorities, you… more
- Medtronic (Mounds View, MN)
- …experience in product development, training, or a related field. + Experience in the medical device industry or a regulated environment is preferred. + Broad ... and techniques. Collaboration and Communication: *Partner with cross-functional teams, including Quality , Regulatory , and R&D, to ensure alignment on training… more