Senior Regulatory Affairs Specialist

Job Summary

A company is looking for a Senior Regulatory Affairs Specialist to support the Medical Solutions Regulatory Affairs team.

Key Responsibilities

• Support new and modified product development projects by integrating regulatory strategy
• Lead the preparation, submission, and maintenance of global product registrations
• Collaborate with internal departments to assess international registration requirements and develop strategies

Required Qualifications

• Bachelor's degree or equivalent work experience preferred
• 1-3 years of Regulatory Affairs experience, preferably in the Medical Device industry
• Strong proficiency in Microsoft Office Applications preferred
• Ability to manage multiple projects with strong organizational skills
• Experience in interpreting and evaluating proposed regulations for medical devices