- 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
- Medtronic (Minneapolis, MN)
- …disease - so their patients can get back to enjoying what they love. The ** Regulatory Affairs Specialist ** will provide worldwide regulatory affairs ... and Class III medical devices including combination products. The Regulatory Affairs Specialist is responsible...with a minimum of 2 years regulatory affairs , quality or engineering + Or an 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
- 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
- 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