Responsibilities:- 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 aQC 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.- 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.