Global Medical Device Regulatory Affairs Specialist
Broughton Group
Broughton Group is seeking a Specialist in Regulatory Affairs based in Noblesville, IN. The role involves obtaining product registration approvals and ensuring compliance with regulatory standards. Candidates should possess a Bachelor’s degree in Life Sciences and a minimum of 3 years of regulatory affairs experience, specifically within the medical device sector. The position requires preparing and maintaining regulatory documentation for global submissions while collaborating with key departments. The role is situated in a manufacturing environment, exposing employees to various workplace hazards controlled for safety. #J-18808-Ljbffr Broughton Group
Vacancy posted 3 days ago
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