Regulatory affairs specialist i

Coordinate, compile, and submit regulatory filings for new and modified products to Costa Rica and Central America Health Authorities. Review of product and manufacturing changes for compliance with applicable regulations and impact to regulatory filings. Monitor and assess regulatory updates for compliance with applicable regulations and impact to regulatory filings, communicate relevant changes to internal stakeholders, and other responsibilities.

Necessary requirements:

Education: Bachelor’s degree in Life Sciences (Pharmacy, Biochemistry, Biomedical Engineering or associated areas)

Experience: 1-3 years of experience as a Regulatory Affairs Specialist in medical devices

English level: B2

Profesional

Bachillerato universitario

Farmacia

Ingeniería Eléctrica - Electromecánica Electrónica y Mecatrónica

Ingenierías Otras

Ingeniería Química

1 año de experiencia

1 Vacante