• Day to day provision of support in the compilation of general regulatory project documents, product labelling, new and/or lifecycle applications to regulatory authorities, and responding to questions received from regulatory authorities.• Managing multiple projects, of benefit to the company.• Providing support to the in country regulatory teams across EMEA.• Contribute to Global Regulatory Strategies and implementation plans, ensuring an aligned EMEA position is… Show more • Day to day provision of support in the compilation of general regulatory project documents, product labelling, new and/or lifecycle applications to regulatory authorities, and responding to questions received from regulatory authorities.• Managing multiple projects, of benefit to the company.• Providing support to the in country regulatory teams across EMEA.• Contribute to Global Regulatory Strategies and implementation plans, ensuring an aligned EMEA position is reached and agreed for assigned project/s• Monitor progress/variance of regulatory plans and communicate as necessary ensuring identified risks are addressed• Partner with project teams and other Consumer Health functions (global manufacturing, marketing, technical groups, country affiliates) to ensure required regulatory activities (pre- and post-licensing) meet business standards, objectives and timelines.• Help to maintain systems, processes and procedures relating to regulatory strategy, ensuring compliance with internal Pfizer policies Show less