Senior Technical Documentation Analyst – R&D

If you identify with our purpose of promoting access to health so that all people can live longer and better and want to work in an entrepreneurial, innovative, ethical, and sustainable company, we want to invite you to participate in our selection process. Come be part of Eurofarma, one of the best companies to work for in the country, according to #GPTW! We value our people and believe that a good experience in the company is the key to success so that we can offer the best products and medicines to our consumer. Here you can be who you are. Everyone is welcome! #VemSerEuro #SomosEurofarma #GrupoEurofarmaResponsibilities and dutiesCheck out the main daily activities for this position:Evaluate, consolidate, and review the technical documentation generated by the R&D areas for the preparation of registration and post-registration dossiers for medicines destined for ANVISA, FDA, EMA, and LATAM markets, ensuring technical and regulatory compliance.Act as a technical-regulatory reference for drug development documentation, promoting the interface between R&D, Regulatory Affairs, Quality Assurance, and other areas involved in the projects.Assist in continuous improvement initiatives for the Technical Documentation area, including document standardization, implementation of checklists, process review, document management, and development of tools that increase efficiency, quality, and the company's readiness for regulated markets.Requirements and qualificationsWe are looking for professionals who meet the requirements below:Completed higher education in Pharmacy, Chemistry, or related areas.Advanced or fluent EnglishEspanhol intermediateKnowledge of drug production, product development, analytical methods, and drug stabilityExperience in continuous improvement initiatives, process standardization, and document management will be considered a differentiator.Knowledge of national and international legislation and regulatory requirements, including ANVISA, FDA, EMA, LATAM markets, Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP).Additional informationAt Eurofarma, we value and support our people throughout their journey! See what we offer you and get to know our main benefits:Medical assistance;Dental assistance;Food vouchers;Internal restaurant;Transportation voucher/Chartered bus/Parking - according to the work unit;Pharmacy/Dispensary with free medicines for you, parents, spouse, and children;Life insurance;Private pension so you can plan your future;Do you have children? You will be entitled to daycare (depending on the work unit);Beauty salon so you can take care of yourself;Gym to take care of your health;Short Friday to enjoy the day as you wish (6-hour workday for employees who do not work in shifts);Development programs, which offer partnerships with educational institutions with discounts;Maternity leaveLocation: Itapevi - SPSchedule: Adm/Flex