MedTech Regulatory Affairs Strategist

Katalyst CRO in the United States seeks a Regulatory Affairs professional to support submissions and ongoing compliance for medical device development and sustaining projects. You will coordinate US/EU filings, develop regulatory strategies, and guide teams through submissions and changes. Collaborate with reviewers, manage labeling reviews, and support quality initiatives under the BSC policy framework. A bachelor’s degree and relevant regulatory experience are required. #J-18808-Ljbffr Katalyst CRO