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