- Abbott (Plymouth, MN)
- …and get on with their lives. **The Opportunity** Abbott is seeking a passionate, experienced ** Regulatory Affairs Specialist II** to join our team on-site in ... including those set by the FDA or other worldwide regulatory agencies to various international affiliates. +...math, engineering, or medical fields. + Master's degree in Regulatory Affairs . + Regulatory experience… more
- Teleflex (Maple Grove, MN)
- Senior Regulatory Affairs Specialist **Date:** Jan 9, 2026 **Location:** Maple Grove, MN, US **Company:** Teleflex **Expected Travel** : Up to 10% ... a difference in patients' lives. **Position Summary** The Sr. Regulatory Affairs Specialist (SRA) will...equivalent work experience. * 5+ years of Medical Device Regulatory Affairs experience, domestic and international… more
- Abbott (Plymouth, MN)
- …on with their lives. **The Opportunity** Abbott is seeking a passionate, experienced **Senior Regulatory Affairs Specialist ** to join our team on-site in ... guidance and expertise on complex worldwide strategies with the help of international regulatory affiliates. + Compile, prepare, review and submit medical… more
- Schwan's Company (Marshall, MN)
- …to quality, innovation and the power of food to bring people together. The Regulatory Affairs Specialist , based out of Bloomington, MN or Marshall, ... product labeling that complies with FDA, FSIS, FNS, and international regulations. This role provides regulatory expertise...or related field + 3+ years' experience in food regulatory affairs , labeling, and nutrition compliance +… more
- Medtronic (Minneapolis, MN)
- …innovation in a more connected, compassionate world. **A Day in the Life** **SENIOR REGULATORY AFFAIRS SPECIALIST ** **Onsite** At Medtronic, we bring bold ... provide. Therefore, we are looking for a passionate **Senior Regulatory Affairs Specialist ** who has...Day In The Life** + Team with business unit Regulatory Affairs Specialists (RAS) and international… more
- Sumitomo Pharma (St. Paul, MN)
- …ensure system validation is maintained. + Work closely with Clinical Operations and Regulatory Affairs to ensure compliance with regulatory requirements. + ... follow us on LinkedIn. The Trial Master File (TMF) Specialist will be responsible for ensuring that SMPA studies...transfer of TMF is sufficient to support any potential regulatory filings. + Champion best practices for building and… more
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