.Regulatory Affairs Manager Spain: About the jobYour Mission: Join Sanofi CHC team for a Regulatory Affairs Manager Spain role! You will work closely with the local business to support delivery of business objectives within the regulatory framework as well as provide excellent knowledge and expertise of the CHC regulatory environment. You will be able to develop and maintain contact with Health Authorities, other Regulatory Bodies as well as participate in events with the local self-care trade associations committees.Our Team: At Sanofi CHC, we have one shared purpose - we work passionately, every day, to 'serve healthier, fuller lives. Our marketing philosophy is driven by this purpose and everything we do is centred around people - our consumers, our customers, healthcare professionals, and our employees - across the world. We are building brands that serve 2bn consumers worldwide, so that they can live healthier, fuller lives. In order to do this better than anybody else, we aspire to become the most consumer-centric Consumer Healthcare company.As a top 3 global CHC player, we want to raise the bar in terms of our strategic and operational capabilities to enable sustainable, above-market growth. In order to achieve this, we need strong talents that will help us shape the future of CHC while sharing our core values of courage, teamwork, respect, and integrity.Main responsibilities:Ensure timely submission and successful registration of new OTC medicinal products in line with local requirements, aligned with local registration strategy within Global Department GRA.Provide regulatory assessment of NBO local implementation and enforce the local NBO execution (innovation).Ensure timely notification of foods/ food supplements, cosmetics and medical devices.Maintenance of existing national Marketing Authorisations and notifications in line with local requirements and global standards.Participate in Artwork change management and approval in order to ensure the compliance of the packaging information.Knowledge of the regulatory legislation to the different products under responsibility.Responsible to keep RA Head informed of new regulations and its impact as soon as informed.Perform regulatory impact assessment.Ensure that updates or new regulatory requirements are reflected in the internal Databases so that these are addressed.Establish, develop and maintain good relationships with relevant National Regulatory Authorities and other bodies/organizations/key stakeholders to facilitate and develop effective collaboration on all regulatory interactions and promote the interests of Sanofi.Participate in some relevant Trade Associations Committees in order to get knowledge in first line about trends, planned new legislations and guidelines