Regulatory Affairs Specialist ()

Monitor and provide guidance on European Union medical device regulations as the subject matter expert, ensuring device certification process compliance, and coordinating with internal teams to address future developments.

Education and Experience Requirements

Bachelors degree in Pharmaceutical Sciences or related.

Special Skills Requirements

Two (2) years of experience evaluating European Union Regulatory compliance, analyzing regulatory trends, and managing regulatory affairs projects.

Partial Telecommuting is permitted

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Thank you.