Regulatory Affairs Officer

Job DescriptionOverall Job Purpose:The Regulatory Affairs (RA) Officer is primarily responsible for ensuring the appropriate licensing, marketing and legal compliance of Sun Pharma’s pharmaceutical and medical products in order to control the safety and efficacy of these products. The RA Officer combines scientific, legal and business knowledge to ensure Sun Pharma’s products meet the required legislation. He/she is responsible for the approval and registration of Sun Pharma’s products in UK market.Responsibilities:Is responsible for liaising with internal and external partners to receive the necessary documents in a timely manner, e.g. internally with R&D, RA and art work departments, externally with translations services and consultants for e.g. Package Leaflet User test reports.Is responsible for the preparation of SmPC, labelling and PILs texts according to the Quality Review of Documents (QRD) format.Is responsible for text verification of the product information documents.Is responsible for proof reading of art work of packaging materials.Ensure dossier technical content is optimal and aligned with UK Regulatory data requirements for new UK Marketing Authorisation ApplicationsMaintains the life cycle management of the dossiers or the approved marketing authorizations as required by submitting variations/notifications/PSURs and renewals.Liaises with regulatory colleagues in the different country offices, corporate groups and competent authorities (MHRA) and third parties on regulatory issues.Works closely together with internal customers such as Research & Development, Artwork, Pharmacovigilance, Quality Assurance, Logistics, Finance, Business Development, Sales.Maintains RA archives (electronically).Keeps the Regulatory Information correct and accessible for other stakeholders.Being able to work with the required IT standards, like eCTD, XEVMPDBeing able to work with the corporate IT systems like AMS, Trackwise, eDMS, eLMS, OneHRDetermines and writes standard operating procedures.Qualifications:Bachelor or Master Degree (preferably in Life Sciences, Languages or Law)Rounded knowledge of the UK and EU Regulatory Framework (directives, regulations, guidelines)Some understanding of the drug development processAble to comply with company standard operating proceduresGood verbal and written communication skills in EnglishGood IT skills including familiarity with Microsoft Office packages and specific packages/portals such as eCTD software, XEVMPD software, TVT, CESP, EMA gateway, MHRA and CBG portal.Excellent attention to detailGood time management skillsGood organization and project management skillsGood interpersonal and team working skillsPresentation skills and experience of delivering training