- Danaher Corporation (Chaska, MN)
- …departments Preferred Skills: + Experience creating artwork for packaging in the Medical Device or Pharmaceutical environment including regulated industries. + ... documents including labels, instruction for use, box artwork, graphics etc. from project initiation through completion. + Create, review, and proof documents for… more
- Medtronic (Mounds View, MN)
- …within the CV Portfolio + Proficient in systems - SAP, OneStream + Medical device experience **About Medtronic** Together, we can change healthcare worldwide. ... portfolio where teams are experiencing critical resource shortages or where specific project /process support is required. The ideal candidate should be a proven… 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 ... on systems within a service area as directed by the Area Service Manager . **Company Overview** At FUJIFILM Healthcare Americas Corporation, we're on a mission to… more
- Medtronic (Mounds View, MN)
- …IT delivery or a related role within a large organization. Experience in the medical device or healthcare industry is a plus. **Skills:** + Deep business ... LIVES** Sr. IT Director for Quality, Regulatory, Clinical, & Medical Sciences (QRCMS) IT Solutions at Medtronic will serve...ensure IT initiatives are aligned with business needs. + ** Project Management:** ** ** Accountability to the overall IT… more
- Medtronic (Fridley, MN)
- …interactive and insightful reports and dashboards using Power BI + Experience in the medical device industry + Experience with 19 Code of Federal Regulations (19 ... Life** The Senior Import Analyst performs analysis and executes project and transactional needs within the US and Canada...computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions… more
- Medtronic (Minneapolis, MN)
- …+ Knowledge and apply this knowledge to post market surveillance of products. + Medical device experience; or experience in a regulated environment + Experience ... and expectations of Regulatory Bodies. This is a scientific (engineering, technical, medical ) writing position. This individual will partner with other teams such as… 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 ... Knowledge Base articles. + Maintains an expert working knowledge of current medical imaging products and related technologies. + Engineers must have the ability… 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 ... customer surveys, documentation accuracy and consistency, timely case and project completion, and finishing the assigned trainings are standard...level of success with yearly goals provided by your manager and metrics defined on a team level. +… more
- Medtronic (Mounds View, MN)
- …selection, processing, analysis, biostability, and process-property-performance relationships for medical devices. Additionally, the individual will serve as a ... your discipline. + Experience with drug discovery and formulation development for device led combination products + Hands on experience designing benchtop testing… more
- Medtronic (Plymouth, MN)
- …years of compliance experience, or an advanced degree. **Nice to Have:** Medical Device background Grant proposal and administration experience **About ... and life-enhancing therapies. **A Day in the Life:** + Monitor program/ project /system status, budgets, and deadlines to ensure smooth operations. + Conduct… more