- Medtronic (Minneapolis, MN)
- …in a more connected, compassionate world. **A Day in the Life** The Senior Regulatory Affairs Specialist (Sr. RAS) is responsible for collaborating, planning ... and review process + Provide business and product information to the international regulatory affairs team to enable development and strategies and… more
- Abbott (St. Paul, MN)
- …female executives, and scientists **The Opportunity** We are seeking a **Principal Regulatory Affairs Specialist ** to join Abbott's Vascular Division ... vascular disease. As an experienced individual contributor, a Principal Regulatory Affairs Specialist is to...Prepares robust regulatory applications for FDA and/or international regulatory agencies to achieve departmental and… more
- Medtronic (Minneapolis, MN)
- …Regulatory Affairs Specialist ** is responsible for developing regulatory strategies, preparing US and international submissions and obtaining and ... maintaining approval for products. Additionally, the Senior Regulatory Affairs Specialist is responsible...**Duties and Responsibilities** : + Collaborate with Operating Unit Regulatory Affairs Specialists and international … more
- Abbott (Plymouth, MN)
- …health and get on with their lives. **The Opportunity** We are recruiting for a **Senior Regulatory Affairs Specialist ** to join our team on-site in our St. ... skills, as well as attention to detail. **Preferred** **Qualifications** + Master's Degree in Regulatory Affairs and may be used in lieu of direct regulatory… 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
- Medtronic (Minneapolis, MN)
- …to healthcare consumers and providers worldwide. **Careers That Change Lives** The ** Regulatory Affairs Specialist ** develops strategies for worldwide ... with other functional resources, such as marketing, global supply chain, etc. Maintain regulatory affairs product files to support compliance with regulatory … more
- Abbott (Plymouth, MN)
- …+ Prepares robust regulatory applications (either for FDA or for international regulatory agencies) to achieve departmental and organizational objectives. + ... including those set by the FDA or other worldwide regulatory agencies to various international affiliates. +...+ Experience working in the Medical Device industry. + Regulatory Affairs Professionals Society Certification is a… more
- Medtronic (Minneapolis, MN)
- …for this opening will close on - 11 Apr 2025 Position Description: Senior Regulatory Affairs Specialist for Medtronic, Inc. Minneapolis, MN. Responsible for ... developing regulatory strategies, preparing US, EU, and international ...related field. Requires two (2) years' experience as a Regulatory Affairs Specialist , R&D Engineer… more
- Abbott (St. Paul, MN)
- …people with diabetes from routine fingersticks. The Opportunity We are currently hiring a Regulatory Affairs Operations Specialist I to work on-site at our ... . Complies with US Food and Drug Administration (FDA) regulations, international regulations and other regulatory requirements, company policies, operating… more
- Bio-Techne (Minneapolis, MN)
- …the work. + Requires 0 to 5 years of experience in Quality Assurance and/or Regulatory Affairs . + The candidate must be self-motivated and must have strong ... to maintain and grow R&D Systems Quality Management System in alignment with international quality and regulatory standards. This position is responsible for… more
- Medtronic (Minneapolis, MN)
- …to the Director of Medical Science, the **Senior Medical Science Specialist ** is responsible for leading clinical evidence development for Peripheral applications ... treatment community. + Therapy-specific expertise The Senior Medical Science Specialist must be detail-oriented and self-motivated, with excellent analytic,… more
- Actalent (Plymouth, MN)
- …interaction, ergonomics, usability, data collection and analysis, reports and analysis, regulatory affairs , risk analysis, medical device Top Skills Details ... to develop processes and procedures that align to initiatives and FDA/ international human factors standards * Providing technical supervision to less experienced… more