Regulatory Affair Medical Device

Professional Summary

Strongly reliable and focused Regulatory Affairs Specialist with great depth and breadth of experience in medical device review and evaluation. Superb multitasker able to handle multiple projects efficiently and accurately. Effective independent worker as well as excellent coordinator with other members of a regulatory affairs team.

Core Qualifications

Extensive experience in quality assurance and regulatory affairs work environments

Superior expertise in medical device regulations and reporting

Excellent proficiency with software tools and metrics

Strong knowledge of testing practices and principles

High skills in maintaining professional relationships with all levels of staff

Outstanding analytical and problem-solving abilities