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Venus Concept
Regulatory Affairs Associate
Remote · Boston, Massachusetts, USA · Full time · Mid level
$85k / year
About the role
Support global registrations and ensure medical devices meet regulatory requirements. Execute regulatory strategies and provide guidance on global markets.
What you’ll do
• Execute regulatory strategies for medical device registration. • Prepare and submit regulatory documents. • Coordinate with in-country regulatory partners. • Provide guidance on regulatory matters. • Stay updated on global regulatory changes.
What you’ll bring
• Bachelor's degree in scientific or technical discipline. • 2-5 years regulatory affairs experience. • Knowledge of global medical device regulations. • Experience with regulatory filings and documentation. • Excellent communication and organizational skills.
Life at Venus Concept
Comprehensive benefits from Day 1 including medical, dental, vision, life insurance, and 401(k) match. Inclusive culture fostering innovation and diversity.
About Venus Concept
Venus Concept is a global leader in medical aesthetic technology with products in over 60 countries and backed by leading healthcare investors.