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Katalyst CRO

Senior Medical Device Regulatory Affairs Specialist

Katalyst CRO, Chicago, Illinois, United States

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A medical device regulatory consultancy in the United States is seeking a Regulatory Affairs Specialist. The role involves obtaining and maintaining regulatory approvals, developing strategies for market clearance, and ensuring compliance with regulatory standards for medical devices. Candidates should possess a Bachelor of Science degree and 5-7 years of experience in regulatory affairs, preferably in the respiratory devices sector. Strong analytical and communication skills are essential for this position. #J-18808-Ljbffr