Responsibilities: • Compile labeling, brochures/catalogs, technical information for product registration. • Coordinate and collect specific registration information with R&D, Manufacturing, QA, Sales. • Request CFG (certificate to foreign government) from the FDA • Obtain legalize documents from County, State, Federal and consulate/embassy • Support International Registrations as it relates to product changes and/or new product launches • Ability to work with minimal supervision. Minimum Requirements • 3 years Regulatory Affairs experience in medical device companies Preferred Qualifications: • International product registration experience preferred. • Proficient in using Microsoft Word, Excel and PowerPoint. • Strong communication and project management skills. • Must be able to handle multiple tasks and attention to detail. • Bilingual is a plus (Spanish) Apply Here
PI129635186
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