Especialista de Asuntos Regulatorios

Ensure compliance with local and international regulations for medical devices. Prepare regulatory submission files for new products and modifications. Manage communication with international regulatory specialists for technical documentation. Analyze local standards and international regulations to ensure compliance.

Bachelor's degree in Pharmaceutical Biology, Biomedical or related fields. Minimum 3-5 years of experience in Regulatory Affairs. Advanced level of English (oral and written) is mandatory.

Professional development opportunities with an international company recognized as a great place to work. Access to a supportive work environment that values diversity and inclusion.