Practicante - Asuntos Regulatorios [Pharmaceuticals / Medical Devices] **This is not a legal/law position**

                Job description
ASUNTOS REGULATORIOS / REGULATORY AFFAIRS
Practicante (tiempo completo, 40h por semana)
Based in/localizado en: Hybrid (office in Lima, Peru) / Remoto + Oficina en Lima Peru.
We are an innovative Peruvian small yet innovative firm that provides comprehensive regulatory affairs solutions for health products (drugs, devices, etc.) for the Latin America region, with a special focus on the "smaller", somehow underserved, markets. We primarily serve the biotechnology, pharmaceutical, and medical device industries but have led successful projects for cosmetics and foods and supplements. Most of the services we provide are related to marketing approvals ("registros sanitarios") and lifecycle management activities in the region, with more than 80% of our submissions made outside of Perú.
We are looking for a recently graduated professional (i.e., complete undergraduate coursework), in the fields of pharmaceutical sciences/pharmacy, toxicology, bioengineering, or related fields, who is looking for an internship (prácticas pre-profesionales, o practices profesionales) that is interested in learning about the regulatory framework for drug products and medical devices.
This role will support regulatory activities for drug products and medical devices, while also providing administrative support related to documentation management, tracking of regulatory submissions, and assist in the coordination of internal teams and external stakeholders.
The ideal candidate is highly organized, detail-oriented, self-motivated, and eager to learn.
The position includes all statutory employment benefits in Peru, such as health insurance (EsSalud), paid annual leave (30 days), severance compensation (CTS), and other applicable benefits.
Candidate Profile
· Intermediate level of English (or higher) as second language.
· Be able to work full time (40 hours/week).
· Complete undergraduate training in pharmacy, toxicology, bioengineering, or related fields. This is not a position for law professionals.
· Experience: No prior experience in regulatory affairs is required. Previous experience or training in the area is advantageous.
· The candidate should be computer literate. The work requires extensive use of productivity applications.
· The candidate must be proactive and have the ability to adapt to changes in environment and priorities as the business requires. We are a small business that needs to move fast and adapts to different client cultures and styles.
· The candidate must have excellent oral and written communication and the ability to interpret complex written information. Although we do provide guided training, a significant degree of self-training from the employees is required. Reading comprehension capabilities are critical.
· Ability and attitude to learn fast.
· Ability to integrate and demonstrate integrity and accountability throughout the organization and externally,