Senior Regulatory Affairs Specialist
Katalyst CRO
Katalyst CRO in Chicago seeks a Regulatory Affairs Level III (Senior Specialist) to manage global product registrations and ensure compliance in the medical device sector. The role involves developing regulatory strategies, leading 510(k) submissions, and supporting quality management systems. Ideal candidates have a Bachelor’s degree and over 5 years of relevant experience, particularly with respiratory devices. Strong analytical, communication, and regulatory knowledge are essential. Join a dynamic team focused on regulatory excellence. #J-18808-Ljbffr
Vacancy posted 2 days ago
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