**Job Title:** Regulatory Affairs Specialist
This role offers an opportunity to develop your career in the Regulatory Affairs sector. You will be responsible for providing administrative support to regulatory staff, filing and tracking documents, responding to requests, and managing files.
About the Role:
As a Regulatory Affairs Administrator, you will work in a small team environment and perform various tasks such as general administrative skills, data entry, proofreading, and compiling reports. You will also manage the regulatory admin inbox, schedule meetings, and provide meeting support as needed. Additionally, you will communicate with internal and external personnel, prepare and maintain documentation, and support regulatory staff with submissions to regulatory authorities.
Requirements:
Minimum of degree qualification in relevant Science, Engineering or Quality Assurance discipline. 1+ years experience working in a Quality Assurance regulated medical product environment is an advantage. Strong interpersonal skills, ability to communicate well verbally and in writing, excellent attention to detail, and ability to prioritize.