.Based in Mexico (remote)Salary: Competitive + Bonus + BenefitsIf you are an agile, committed, and innovative regulatory affairs professional in the pharmaceuticals sphere, then we want to hear from you!Join us to help improve peoples' lives and make healthcare better for everyone!Why Pharmanovia?Pharmanovia is a dynamic, fast-growing international pharmaceutical company with a portfolio of over 20 brands across more than 160 markets. Our mission is to improve patient health globally through the revitalisation of niche, tried-and-trusted medicines.Our Core Behaviours AreWe act decisively but we never compromise on quality.We keep our promises and do as we say.We value our heritage and foster an entrepreneurial spirit.We reinvest in our future – in our products, our brands, and our people.We give back to our communities.Since its inception in 2013, Pharmanovia has grown consistently year on year, focusing on delivering high-quality branded prescription medicines to patients, prescribers, and healthcare providers across the world. Our growth has enabled the company to reinvest in its products, brands, people, and to give back to its communities. A people business with a strong, supportive culture that encourages innovation and entrepreneurial spirit, our team comprises over 300 employees and 29 nationalities, operating from offices in the UK, Denmark, Netherlands, Switzerland, U.A.E., India, Singapore, Italy, Spain, and South Korea.We are an agile, committed, and innovative global specialty pharma business and a preferred partner for innovator pharma companies, instigating a paradigm shift in the life cycle management of iconic medicines. We seek to extensively engage with clinical communities to communicate product improvements and prioritise environmental, social, and governance considerations across the business and workforce.Pharmanovia's therapeutic areas include Cardiovascular, Oncology, Endocrinology and Neurology.About The RoleReporting to the Global RA Lead, as Regulatory Affairs Manager (or Senior Manager, depending on experience) you will lead the establishment of Regulatory Affairs management in the LATAM region.Responsible for all aspects of the LATAM Regulatory Strategy, you will support the growth of the pipeline in LATAM. In this role you will work closely with the Global Regulatory Lead, Regulatory Product Leads, Scientific Affairs and General Manager in cross-functional project teams, to ensure LATAM growth strategies are realised.Our Regulatory Affairs Department has an ethos of continuous improvement, refining systems and creating efficiencies. This, along with the rapid growth of the business, leads to a varied and dynamic working environment