Regulatory Affairs Coordinator

Coordinate activities with Area Therapeutic Area Teams and local stakeholders to ensure compliance with local regulations for marketing authorization applications. Review and validate translations of documents and prepare files for submission to the local Health Authority. Maintain the archive of legal documents and ensure the validity of GMPs and other regulatory documents throughout the marketing authorization lifecycle.

Bachelor's degree in Pharmacy, Biotechnology Engineering, Pharmaceutical Engineering, or a related field. 2 to 5 years of experience in a similar position. Knowledge of health regulations in Mexico and fluency in English, both written and spoken.