Work cross-functionally with different departments including R&D, Marketing, and Quality Assurance to assist in regulatory decision-making and develop a broad understanding of the medical device industry
Perform Regulatory Intelligence activities to ensure the regulatory strategy remains optimally efficient amidst changing regulations and global expansion
Assist in building and maintaining Regulatory Files/product technical documentation for product registrations
Prepare various regulatory submissions for registering products globally to ensure products can reach our customers and patients.
Required Skills
Currently working on or recently completed a Master's degree in a related field or equivalent;
Excellent written and verbal communication skills
Strong interest in Regulatory Affairs
Ability to work independently
Skilled with Microsoft Word, Excel, Powerpoint and Adobe Pro