Payal Lanje

At Capgemini, I managed FMCG artwork data orchestration for product launches, reviewing and approving labels, packaging, and artwork for compliance across regional markets. I maintained an artwork and regulatory data repository, tracked milestones across concurrent projects, and verified product claims, ingredient declarations, warnings, and instructions for use. At IQVIA, I prepared and maintained regulatory dossiers and eCTD-compliant submission packages for FDA and EMA filings, including INDs and clinical study documentation. I also reviewed labelling components and supported artwork approvals against FDA, EMA, and ICH guidelines. At GlaxoSmithKline (GSK), I supported global regulatory labelling activities, maintained version-controlled documents, and assisted with linguistic reviews and translation validation. I’m seeking a UK-based Regulatory Affairs role in pharmaceuticals, medical devices, food supplements, nutraceuticals, cosmetics, or consumer healthcare.