Job Summary

A company is looking for a Regulatory Affairs Specialist.

Key Responsibilities:

• Maintain and expand product lines
• Provide planning and technical support for regulatory submissions
• Monitor, interpret, and assure compliance with regulatory requirements

Required Qualifications:

• Bachelor's degree in a relevant scientific discipline
• 2+ years of experience in medical devices and regulatory affairs preferred
• Ability to manage complex projects in a team environment
• Scientific knowledge and technical system skills
• Proofreading and editing skills