REGULATORY AFFAIRS ANALYST

Description

Job Summary: We are seeking a Regulatory Affairs Analyst to ensure effective interaction with the local Health Authority, regulatory compliance, and documentary support. Key Responsibilities: 1. Manage and track regulatory procedures and inquiries 2. Ensure compliance with local sanitary regulations 3. Prepare and submit Sanitary Registration dossiers **REGULATORY AFFAIRS ANALYST** Job Description: **Publication Date:** March 18, 2026 **Salary:** S/3,000\.00 \- S/3,300\.00 per month Job Description: **We are currently seeking a professional for the position of: REGULATORY AFFAIRS ANALYST** **Responsibilities:** Ensure effective interaction with the local Health Authority to monitor ongoing procedures and evaluate and resolve inquiries related to regulatory activities. Ensure compliance with local sanitary regulations for promotional materials, as well as for the proper commercialization and distribution of registered products in countries under responsibility. Provide regulatory documentary support for tendering and commercial processes. Ensure business continuity through management of changes in sanitary registrations due to product or associated document modifications. Ensure timely internal notification upon approval of procedures by the Health Authority for product commercialization. Ensure maintenance and proper storage of sanitary registration files authorized by the health agency for authorship and local regulatory compliance purposes. Prepare, plan, coordinate, supervise the preparation and submission of Sanitary Registration dossiers (new registrations, transfers, modifications, renewals, corrections, authorizations, advertisements, and responses to preventive measures) for divisional products (pharmaceuticals and medical devices) submitted to the health authority and approved distributors in assigned countries, aligned with business strategy. Ensure adherence to departmental procedures. Establish and foster teamwork with internal clients (Manufacturing, Marketing, Sales, Finance) and external providers (translators, IT service providers, regulatory consultants, etc.) to ensure smooth functional execution. **Qualifications/Experience:** Bachelor’s or licensed Pharmaceutical Chemist (mandatory) Minimum 1–2 years of experience in the regulatory area for medical devices. Knowledge of national regulations · Adaptability and teamwork skills. · Intermediate-level English proficiency (conversational). Proficiency in Excel. · Experience in tenders (not mandatory) · Willingness to work in Lince · Working hours: Monday to Friday, 8:00 AM to 6:30 PM. Employment Type: Full-time Work Location: On-site employment Employment Type: Full-time Work Location: On-site employment Salary: S/.3,000\.00 \- S/.3,300\.00 per month Work Location: On-site employment