- Fujifilm (St. Paul, MN)
- …progressive experience as a Technical, Systems , Software or Quality Assurance Engineer in Medical IT and/or Imaging products. + Exceptional communication and ... but not limited to: storage, PACS, VNA, Mobility, 3D Systems , Syncomm and Clinical Information Systems for...all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485… more
- Abbott (St. Paul, MN)
- …experience in software or systems engineering + 3+ years' experience in Medical device development and/or other highly regulated industry. + Sound decision ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more
- Medtronic (Fridley, MN)
- …to enhance collaboration and ensure successful completion of projects. The Senior Medical Safety Specialist is responsible for providing medical expertise and ... Quality/Post-Market Vigilance, Regulatory, and Clinical. You will apply your medical knowledge, clinical expertise, and product knowledge to support patient… more
- Medtronic (Minneapolis, MN)
- …M&T Structural Heart Business is one of the fastest growing businesses in the medical device industry and expanding rapidly to serve patients globally. The ... Serves as a technical resource to support a specific medical product or solution. + All other duties as...a key role in all aspects of Intrepid TMVR/TTVR device preparation & case support + Provide technical support… 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 ... **Position Overview** The Senior Technical Support Engineer , MI - I (Tier 1) provides highly...the needs of the business, to work on customer systems . + Adheres to the Company's quality and regulatory… more
- Medtronic (MN)
- …experience in a clinical lab setting, clinical training, field sales/support in medical device , healthcare industry or equivalent experience -OR- + Associate's ... relevant experience in a clinical lab setting, clinical training, field sales/support in medical device , healthcare industry or equivalent experience + OR- +… more
- Medtronic (Minneapolis, MN)
- …profile._ + Bachelor's degree in a technical discipline + Minimum 7 Years of medical device regulatory experience with Bachelor's degree + Or minimum 5 Years ... of medical device regulatory experience with an advanced...growth and cross-functional collaboration as we work together to engineer the extraordinary. **Physical Job Requirements** The above statements… more
- Medtronic (Fridley, MN)
- …FDA 21 CFR part 820 requirements and ISO 13485, ISO 14971, European Union (EU) Medical Device Regulation (MDR), and State of the Art (SOTA). Apply probability ... (3) years of experience as a Reliability or Quality Engineer . Experience must include three (3) years of post-Bachelor's...820, ISO 13485, and ISO 14971 European Union (EU) Medical Device Regulation (MDR), and State of… more
- Medtronic (Minneapolis, MN)
- …to expand access for patients. You will possess a strong background in medical device technology, possess product and procedure expertise, therapy development ... retention and fecal incontinence with our sacral neuromodulation (SNM) systems InterStim X (TM) ️ and InterStim (TM) ️...+ 5+ years of experience in a clinical or medical device environment, with a focus on… more
- Medtronic (Minneapolis, MN)
- … device selection, appropriate programming, correct implantation and testing of all device systems ). + Maintains current knowledge about assigned products and ... retention and fecal incontinence with our sacral neuromodulation (SNM) systems InterStim X (TM) ️ and InterStim (TM) ️...personnel on product use + Experience working with a medical device or pharmaceutical company and clinical… more