EU Regulatory Affairs Specialist

A company is looking for a Regulatory Affairs, Advertising and Promotion, EU.

Key Responsibilities

Review and approve proposed advertising and promotional materials for multiple product lines

Maintain current awareness of evolving EU MDR and FDA regulations impacting the pharmaceutical and medical device industries

Oversee timely and accurate submissions related to promotional materials and manage audits for compliance

Required Qualifications

Bachelor's Degree in a scientific background (medicine, pharmaceutical sciences, human biology, or chemistry)

5+ years of experience in regulatory drug and medical device promotion review

Strong knowledge of EU MDR and FDA regulations related to advertising and promotion

Proficiency in Microsoft Office Suite and familiarity with online meeting tools

Experience in monitoring regulatory compliance trends in the aesthetic industry