Regulatory Affairs Associate — CMC & PMA Expert
Katalyst CRO
Katalyst CRO is seeking a regulatory affairs professional to manage CMC dossiers, coordinate PMA submissions, and oversee CTD content for Class III implantable devices. This role requires collaboration with global teams and extensive experience with regulatory submissions. You will lead complex documentation efforts, ensure compliance with US FDA PMA guidance, and drive project timelines across multiple initiatives. #J-18808-Ljbffr Katalyst CRO
Vacancy posted 4 days ago
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