EU Regulatory Affairs Specialist

Job Summary

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