Jennifer Amy Mardones TschidaRecruiter:Jose Daniel Calderon Robles
Hybrid Roles:
About this role:
With adequate supervision, the is responsible for supporting international geographies to gain and maintain EP product approvals.
Your responsibilities will include:
- Prepare and provide appropriate documentation to international Regulatory partners for new product registrations and renewals.
- Prepare and provide appropriate documentation to international Regulatory partners to support change submissions.
- Support international requests for product release in collaboration with Division Regulatory product SME.
- Liaise with international Regulatory partners for various projects as directed.
- Support efforts to continuously improve department and divisional quality, including collaboration, best practices, and knowledge sharing.
What we’re looking for in you:
Minimum Qualifications
- Bachelor’s degree, minimum
- 2-3 years of experience in Regulatory Affairs (R&D, Quality, Clinical, Medical Affairs, Biocompatibility) in the medical device industry
- Proven organizational skills, including ability to manage multiple tasks/requests
- Basic computer skills, including experience with the software applications Microsoft Word, Excel, PowerPoint and Adobe Acrobat
- English proficiency 90%+
Preferred Qualifications
- General understanding of product development process and design controls
- Working knowledge of FDA, EU and international regulations
- Effective problem solving skills
- Effective written and oral communication