- Support the maintenance of regulatory files and tracking databases to ensure prompt and accurate access to company regulatory information (concerning current, pending and future approvals and renewals).
- Assist in reviewing product and process documentation for assigned projects to ensure compliance with requirements, as well as monitor renewals to strict deadlines.
- Stay up to date with the latest rules and regulations.
- Maintaining a regulatory documentation database.
- Ensuring accurate and timely submissions to regulatory agencies.
Bachelor’s Degree in Science, Veterinary, or any related field.From 5-7 years of experience in registration and importation approvals, final release approvals, registration licenses, and scientific committees.Medical device registration experience is a must.Excellent verbal and written communication skillsStrong interpersonal skillsExcellent customer service skillsStrong problem-solving skillsExcellent organizational skillsHighly developed attention to detailAbility to work well in a team environment