Job Title: Regulatory Affairs Jr. Specialist Location: CDMX (Onsite) Employment Type: Full-Time Job Description: Support the preparation, review, and follow-up of regulatory submissions for medical devices, ensuring compliance with applicable regulations before health authorities such as COFEPRIS. The role focuses on enabling timely approvals and maintaining product registrations. Qualifications / Requisitos: • Bachelor’s degree in Chemistry, Pharmaceutical Chemistry, Pharmacy, Biomedical Engineering, Biotechnology, or a 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 the Medical Device industry. Technical Skills: • Experience of Mexican medical device regulations (COFEPRIS) - Must • Medical device classification • Applicable NOMs and standards - Must Have • Intermediate to advanced English (technical reading required) • Intermedia...