Pb Responsibilities: /b /pulli Cross-check scientific information against cited references and ensure accuracy (fact checking) /lili Ensure consistency with approved product labelling and check for any off-label communication /lili Ensure translation accuracy for localized material (against general version) and adherence to approved local label (indications, disease state description, population etc. per local label) /lili Cross check consistency in reference citation style /lili Verify presence of essential information like brand and generic names, AE reporting, presence of API etc, (based on checklist) /lili Reference link and annotate assets in Veeva /lili Liaise with content development team stakeholders and provide clarification on content or references. /lili Ensure quality of review and submission of the jobs within the agreed-upon time frame. /lili Keep themselves updated on different products TAs /lili Provide inputs on metrices such as SLAs, KPIs and other periodic reports. /li /ul pb Requirements: /b /pulli Advanced bioscience or pharmacy/medical qualification. /lili Excellent communication ability, both verbal and written (both, Spanish and English), at all levels /lili Experience in pharmaceutical industry within medical affairs; experience working as a QC reviewer for promotional and non-promotional materials of prescription only medications. /lili Strong scientific acumen and ability to grasp complex therapeutic areas. /lili Good understanding of Global and Local regulations on advertising, promotion and scientific exchange. /lili Good multitasking, project management, team management and organizational skills. /lili 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. /li /ul