LATAM Regulatory Affairs Coordinator/Bilingual

Your Role: Participate, coordinate and support in the execution of projects in Mexico and LATAM countries, through coordination, obtaining, reviewing and supplying technical and legal information for the registration, renewal, modification and maintenance of sanitary records of medicines, on time and in form, to achieve objectives. Responsibilities: Assembling dossiers for new registrations, renewals, modifications, transfers and updating information for prescription drugs, as well as coordinating with regulatory agencies, obtaining and reviewing documentation, and providing support for the registration process. Additionally, you will be responsible for maintaining accurate records of all activities, including tracking and reporting on project progress, identifying and addressing potential issues, and ensuring compliance with relevant regulations and standards. Requirements: Bachelor's degree in a related field, such as life sciences or regulatory affairs, 2+ years of experience in the pharmaceutical industry, fluency in Spanish and English, ability to work independently and as part of a team, strong analytical and problem-solving skills, excellent communication and interpersonal skills, and proficiency in Microsoft Office. Benefits: Competitive salary, comprehensive benefits package, opportunities for professional growth and development, and a dynamic and supportive work environment.