A company is looking for a Regulatory Affairs Specialist.
Key Responsibilities
Create and execute regulatory strategies for post-market activities and design change evaluations
Manage regulatory initiatives and support global regulatory strategies for new product development
Advise business teams on regulatory issues and ensure compliance with IVDR Technical Files
Required Qualifications
Bachelor's Degree with 3+ years of experience in Regulatory Affairs or a Master's Degree with 1+ year of experience
Subject matter expertise in registration and commercialization of in vitro diagnostic medical devices
Experience in the Biotech pharmaceutical industry
Strong Health Canada and EU submission experience preferred
Regulatory Specialist • Van Nuys, California, United States