Job Description Key Responsibilities: Products Provides clear and constructive Europe Region (Area) regulatory input and intelligence to Area and Global Regulatory & Development Project Teams via the Area and/or Global Regulatory Lead (GRL) in accordance with Area & Commercial objectives. Ensure planned drug development activities comply with Area guidelines and if they do not, escalate to Manager and provide a critical analysis of the risks and issues with a remediation proposal. Support global product development strategy(s); outlining options for Scientific Advice/PIP/Accelarated regulatory pathways, co-ordinating preparation of briefing packages and supporting preparation of documents for agency meetings. Outline options for Europe Region filing strategy (including CP, MRP, DCP, National); identifying risks, issues and solutions. Plan, implement and conduct regulatory activities in support of lifecycle maintenance in Area. Identify compliance risks and remediation activities proactively. Support lifecycle maintenance activities including the review of CMC, QRD, PSUR and labelling submissions and approval of product-related packaging as required to ensure regulatory compliance. Implement effective planning, tracking, archiving of activities, especially with regard to submissions, internal memos and key correspondence. Ensure effective planning and tracking of activities via RIM system. People Build strong and effective relationships with Area, Affiliate & Global regulatory & cross functional colleagues to ensure Area and Affiliate RA activities are in line with regional business priorities. Processes Follow core GRS policies and procedures. Support implementation of new processes and input into changes in processes, as required. Responsible for the Notification of Regulatory activities and RIM system entry/data accuracy for allocated projects. With supervision, provide forecasts and actuals and manage in line with regional requirements, communicating these to Area TA Head, GRL and R&D finance for assigned projects. Follow all approved Abbvie Area procedures and guidance.