Design and Development Analyst

Description

Position Summary: Support the Technical Management and Regulatory Affairs process, ensuring compliance with Good Manufacturing Practices (GMP) and current health regulations. Key Responsibilities: 1. Responsible for supporting Technical Management and Regulatory Affairs 2. Ensure compliance with GMP and current health regulations 3. Handle regulatory procedures before INVIMA At Laboratorios Gusing S.A.S., located in San Mateo, Soacha, we are seeking a Regulatory Affairs Analyst who will be responsible for supporting the Technical Management and Regulatory Affairs process, ensuring compliance with Good Manufacturing Practices (GMP) and current health regulations. **Requirements:** * Pharmaceutical Chemist with a valid Professional License. * Knowledge of GMP and GLP. * Knowledge of quality control, stability studies, and product design and development. * Experience handling regulatory procedures before INVIMA (health registrations, modifications, and renewals). * Knowledge of pharmacovigilance. **Experience:** Minimum 1 year in the pharmaceutical sector (certified professional internships are acceptable). **Salary:** To be agreed upon. Immediate availability. Residence in Soacha or surrounding areas. **Working Hours:** Monday to Thursday: 7:10 AM to 5:30 PM Friday: 7:10 AM to 4:00 PM **Job Type:** Full-time. Job Type: Full-time Work Location: On-site employment