.**Job Description**:Regulatory Affairs Specialist, Export Countries (Solventum)Mexico City3M Health Care is now SolventumAt Solventum, we enable better, smarter, safer healthcare to improve lives. As a new company with a long legacy of creating breakthrough solutions for our customers' toughest challenges, we pioneer game-changing innovations at the intersection of health, material and data science that change patients' lives for the better while enabling healthcare professionals to perform at their best. Because people, and their wellbeing, are at the heart of every scientific advancement we pursue.We partner closely with the brightest minds in healthcare to ensure that every solution we create melds the latest technology with compassion and empathy. Because at Solventum, we never stop solving for you.The Impact You'll Make in this RoleAs Regulatory Affairs Latam for Export Countries you will have the opportunity to tap into your curiosity and collaborate with some of the most innovative and diverse people around the world. Here, you will make an impact by:- You will be responsible to provide all regulatory support to Consultants and Distributors in Export Countries, in order to assure the compliance with the local regulatory legislation and the Company requirements.- You will be the regulatory contact between the Consultants in Latam export countries (Costa Rica, Panama, Honduras, Guatemala, etc) and 3M Regulatory team in the Headquarter and in the different Sources of Supply in order to provide on the regulatory information required locally to maintain and update sanitary registers, registers new products, provide documents and certificates, etc.- You will be responsible of manage regulatory documents and provide these to Consultants and Distributors: Technical and Legal Documents of registration and bids activities such as Certificate of Foreign Government, Certificates of Free Sale, Good Manufacturing, etc.- You will be responsible of the compile, preparation, and support the submission of dossiers with regulatory purposes in Latam countries assigned for submission of Medical Devices and Drugs- You will carry out the development of Standard Operation Procedures (SOP's) for Regulatory Activities and Tracking with the Consultants and Distributors.- Others: Approvals of Stocks Keeping Units (SKU's) for Supply and Demand Activities. Labelling review and approvals and Advertising review for Marketing campaigns.Your Skills and ExpertiseTo set you up for success in this role from day one, Solventum requires (at a minimum) the following qualifications- College: Degree on pharmaceutical, medical or biomedical- Certificate issued is required