Intern supports RA Specialists with regulatory activities in general from Central America´s countries: Learning at MoHs, processes, regulations, best practices, activities, and projects with LATAM.
Interest in learning regulatory affairs activities and medical devices local regulations.
This role focuses on regulatory operational support, with a wide variety of regulatory tasks working within a collaborative team.
Ensure an understanding of the regulatory process.
Organization / focus on detail / likes to read in detail.
Required qualifications:
Career: Student in Engineering, Pharmaceutical, Chemical, Biotechnology, Biomedical or health related.
Open study area for people interested in the regulatory area.
Knowledge in data automation is preferable.
Coordinate regulatory documentation activities and maintain data in information systems or databases.
Create and execute timely manner the Work Plan for submissions, renewals, and amendments of the regulatory projects and ensure full compliance with regulations of the products in charge.
Support with documentation order and regulatory communications
Evaluate applicable laws and regulations to determine impact on company activities.