Responsibilities: Siga leyendo para comprender completamente lo que este trabajo requiere en cuanto a habilidades y experiencia. Si su perfil encaja, presente su candidatura. - Cross-check scientific information against cited references and ensure accuracy (fact checking) - Ensure consistency with approved product labelling and check for any off-label communication - Ensure translation accuracy for localized material (against global version) and adherence to approved local label (indications, disease state description, population etc. per local label) - Cross check consistency in reference citation style - Verify presence of essential information like brand and generic names, AE reporting, presence of API etc, (based on checklist) - Reference link and annotate assets in Veeva - Liaise with content development team stakeholders and provide clarification on content or references. - Ensure quality of review and submission of the jobs within the agreed-upon time frame. - Keep themselves updated on different products & TAs - Provide inputs on metrices such as SLAs, KPIs and other periodic reports. Requirements: - Advanced bioscience or pharmacy/medical qualification. - Excellent communication ability, both verbal and written (both, Spanish and English), at all levels - Experience in pharmaceutical industry within medical affairs; experience working as a QC reviewer for promotional and non-promotional materials of prescription only medications. - Strong scientific acumen and ability to grasp complex therapeutic areas. - Good understanding of Global and Local regulations on advertising, promotion and scientific exchange. - Good multitasking, project management, team management and organizational skills. xohynlm - Total experience – 2-4 years of pharmaceutical industry experience which includes medical affairs/medical information related content writing, review, literature reviews, publications support etc with 2-3 years of experience in promotional/non-promotional medical review.