PbResponsibilities: /b /pulliCross-check scientific information against cited references and ensure accuracy (fact checking) /liliEnsure consistency with approved product labelling and check for any off-label communication /liliEnsure translation accuracy for localized material (against global version) and adherence to approved local label (indications, disease state description, population etc. per local label) /liliCross check consistency in reference citation style /liliVerify presence of essential information like brand and generic names, AE reporting, presence of API etc, (based on checklist) /liliReference link and annotate assets in Veeva /liliLiaise with content development team stakeholders and provide clarification on content or references. /liliEnsure quality of review and submission of the jobs within the agreed-upon time frame. /liliKeep themselves updated on different products TAs /liliProvide inputs on metrices such as SLAs, KPIs and other periodic reports. /li /ulpbr/ppbRequirements: /b /pulliAdvanced bioscience or pharmacy/medical qualification. /liliExcellent communication ability, both verbal and written (both, Spanish and English), at all levels /liliExperience in pharmaceutical industry within medical affairs; experience working as a QC reviewer for promotional and non-promotional materials of prescription only medications. /liliStrong scientific acumen and ability to grasp complex therapeutic areas. /liliGood understanding of Global and Local regulations on advertising, promotion and scientific exchange. /liliGood multitasking, project management, team management and organizational skills. /liliTotal 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