- Bio-Techne (Minneapolis, MN)
- …for researchers to further treat and prevent disease worldwide. **Position Summary:** The Advanced Regulatory Affairs Specialist provides independent ... support to senior regulatory staff to submit regulatory filings. This position will demonstrate advanced ...Bachelor's degree with 3-5 years of relevant experience in regulatory affairs in an IVD manufacturing environment;… more
- Medtronic (Minneapolis, MN)
- … support for Class I, II and Class III medical devices. The Sr Principal Regulatory Affairs Specialist is responsible for activities to launching new ... diagnosis and treatment of atrial fibrillation. The Sr Principal Regulatory Affairs Specialist will work...of manufacturing and change control, and an awareness of regulatory trends + Advanced degree in a… more
- Philips (Plymouth, MN)
- The Principal Regulatory Affairs Specialist will play a critical role in preparing comprehensive regulatory strategies for complex new devices and post ... for balancing the project risk to project teams and Regulatory Affairs Management. + Lead communication and...of a Bachelors degree (required) in Regulatory Affairs , a technical or business discipline, Advanced … more
- Medtronic (Minneapolis, MN)
- …and efficiently, with more predictable procedure times and outcomes. The **Senior Regulatory Affairs Specialist ** develops strategies for worldwide product ... Ablation Solution portfolio is aligned with existing portfolio. Maintain Regulatory Affairs product files to support compliance...degree + Or minimum 2 years of medical device regulatory experience with an advanced degree **Nice… 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 ... Paul, MN. In this role, you will lead the preparation and submission for regulatory approvals and identify and resolve problems. You will provide regulatory … more
- Medtronic (Mounds View, MN)
- …clinical studies. You will work with the Clinical Management, Clinical Quality, and Regulatory Affairs to satisfy applicable regulatory standards and ... clinical studies. You will work with the Clinical Management, Clinical Quality, and Regulatory Affairs to satisfy applicable regulatory standards and… more
- Medtronic (Mounds View, MN)
- …Product Development, Therapy Development, Manufacturing, Sales & Marketing, Distribution, and Regulatory Affairs + Assists clinical management with other duties ... Day in the Life** As an Echocardiography and Imaging Specialist , you will play a critical role in enhancing...safety, and efficacy of products and to satisfy applicable regulatory standards and Medtronic internal requirements for clinical studies.… more
- Medtronic (Minneapolis, MN)
- …meet regulatory requirements and industry standards, collaborating with regulatory affairs to prepare necessary documentation. + **Stakeholder Engagement:** ... revenue growth. We are hiring a seasoned **Principal Program Marketing Specialist - Indication Expansion** to drive high-impact multi-channel marketing awareness and… more
- Medtronic (Plymouth, MN)
- …+ Drives local evidence dissemination & awareness. + Collaborates closely with medical affairs , regulatory , marketing, and other functions to gather feedback on ... Day in the Life** In this exciting role as a Senior Clinical Research Specialist (CRS) you will have primary responsibility in the development and execution of… more
- Edwards Lifesciences (St. Paul, MN)
- …and how our products transform patients' lives. As part of our Clinical Affairs team, you'll hone your scientific curiosity and passion for evaluating data to ... with principal investigators, dedicated medical professionals, patient advocacy groups, and regulatory authorities, you will drive the evidence needed to optimize… more