- Oracle (St. Paul, MN)
- …driving Oracle's success and competitiveness in the healthcare and life sciences sector. As a Medical Device Regulatory Affairs Strategist, you will work ... with SaMD in areas such as Regulatory Affairs , Quality Compliance, Product Development, etc. in medical... Affairs , Quality Compliance, Product Development, etc. in medical device industry or equivalent. Experience authoring… more
- Teleflex (Maple Grove, MN)
- …in a science or engineering field, or equivalent work experience. * 5+ years of Medical Device Regulatory Affairs experience, domestic and international. ... Senior Regulatory Affairs Specialist **Date:** Jan 9,...- The Interventional business unit at Teleflex offers innovative medical devices that are used to diagnose… more
- Oracle (St. Paul, MN)
- …and industry collaboration around AI in healthcare. Required Qualifications + 8+ years in medical device regulatory affairs or regulatory ... deep regulatory and scientific leadership for AI-enabled medical device solutions. This role sits within...as a reviewer, regulatory scientist, or senior regulatory affairs leader. + Demonstrated experience reviewing… more
- GRAIL (St. Paul, MN)
- …, development, clinical affairs , quality, or program management within the IVD, medical device , or pharmaceutical industries is required. + Regulatory ... FDA and/or global health authorities. + Support the US Regulatory Affairs team in preparing submissions such...and international regulatory frameworks and processes for medical device development and approvals is required.… more
- Abbott (Plymouth, MN)
- …etc.), math, engineering, or medical fields. + Master's degree in Regulatory Affairs . + Regulatory experience with capital equipment including ... the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices , nutritionals and branded generic medicines. Our 114,000… more
- Abbott (Plymouth, MN)
- …of international regulatory affiliates. + Compile, prepare, review and submit medical device submissions to regulatory agencies + Interfaces directly ... affairs function. **Preferred** **Qualifications** + 4+ years of related regulatory submission experience from medical device , pharmaceutical, or… more
- Medtronic (Minneapolis, MN)
- …in the medical device industry, particularly with Class III medical devices (PMA). + ** Regulatory Submission Expertise:** Proven experience preparing ... connected, compassionate world. **A Day in the Life** **SENIOR REGULATORY AFFAIRS SPECIALIST** In collaboration with leading...**To Be Successful in This Role** + ** Medical Device Experience:** Direct experience… more
- ManpowerGroup (Maplewood, MN)
- …of experience in regulatory affairs within the pharmaceutical or medical device industry, including experience with combination medical devices ... Our client, a leading organization in the medical device and pharmaceutical industry, is seeking a Regulatory Affairs Lead to join their team. As a … more
- Minnesota State (St. Cloud, MN)
- …specified Closing Date (if designated).** **Working Title:** Adjunct Instructors - Regulatory Affairs and Services **Institution:** St. Cloud State University ... the St. Cloud State at Plymouth - Department of Regulatory Affairs & Services. Graduate level ...The RAS is a professional Graduate program with a medical device focus that offers a Master… more
- Otsuka America Pharmaceutical Inc. (St. Paul, MN)
- **Job Summary** The Chemistry, Manufacturing and Controls (CMC) Global Regulatory Affairs (GRA) professional is responsible for developing and executing global ... relationships with other local and/or global functional units [OPC CMC Global Regulatory Affairs , Global Regulatory Strategy, Manufacturing facilities,… more
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