Regulatory Affairs Jr. Specialist Consultant

re you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’s the best of both worlds…. ClinChoice is searching for a Regulatory Affairs Associate Consultant for 12 months Contract with possibility of extension to join one of our clients. ClinChoice is a global full-service CRO with a strong focus on quality, professional development, and supportive culture. As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with the client’s counterparts. Regulatory Affairs Jr. Specialist Consultant / Especialista Jr. de Asuntos Regulatorios Location / Ubicación: Ciudad de México, México Position Summary / Resumen del puesto: Support the preparation, review and follow-up of regulatory submissions for medical devices, ensuring compliance with applicable regulations before health authorities such as COFEPRIS, enabling timely approvals and maintenance of product registrations. Apoyar en la preparación, revisión y seguimiento de trámites regulatorios para dispositivos médicos, asegurando el cumplimiento de la normativa aplicable ante la autoridad sanitaria COFEPRIS, facilitando la obtención y mantenimiento de los registros sanitarios. Key responsabilities / Responsabilidades principales: • Prepare and compile regulatory documentation for COFEPRIS submissions (registrations, renewals, changes). • Follow up on submissions with regulatory authority (COFEPRIS). • Support interpretation of local and international regulations. • Support coordination of requests and activities with cross-functional teams. • Maintain updated regulatory files and databases. • Preparar y compilar documentación regulatoria para sometimientos ante COFEPRIS (registros, renovaciones, modificaciones). • Dar seguimiento a los trámites ante autoridad regulatoria (COFEPRIS). • Apoyar en la interpretación de normativas locales e internacionales. • Apoyar la coordinación de solicitudes y actividades con áreas internas. • Mantener actualizados archivos regulatorios y bases de datos. Qualifications / Requisitos: Bachelor’s degree in Chemistry, Pharmaceutical Chemistry, Pharmacy, Biomedical Engineering, Biotechnology, or related field. Licenciatura en Química, QFB, QFI, QBP, Farmacia, Ingeniería Biomédica, Biotecnología o afín. Experience / Experiencia: Minimum 1 year of experience in regulatory affairs, quality or medical device industry. Technical skills / Conocimientos técnicos: • Mexican medical device regulations (COFEPRIS). • Medical device classification. • NOMs and standards aplicable. • Intermediate-advanced English (technical reading required). • Intermediate Excel skills (data tracking, pivot tables, basic formulas, reporting). Core competencies / competencias clave: • Attention to detail. • Organizational and documentation skills. • Effective communication. • Team collaboration • Learning Agility.