Senior Regulatory Affairs Specialist

Job Summary

A company is looking for a Sr. Regulatory Affairs Specialist.

Key Responsibilities

• Collaborate with internal regulatory partners on product development projects and integrate international regulatory strategies
• Maintain regulatory information to support customer queries and submissions
• Provide regulatory support for a range of medical devices and maintain regulatory data and analytics

Required Qualifications

• Bachelor's degree in a related field preferred
• 2+ years of experience in Medical Device Regulatory Affairs/Quality preferred
• Certification in a regulatory affairs program preferred
• Effective project management skills
• Ability to work collaboratively in a team environment