Regulatory Affairs Analyst

Preparing documentation for regulatory processes to be filed with regulatory bodies;
- Renewing licenses for products and establishments before the relevant bodies (MAPA, ANVISA, professional councils,among others), ensuring that processes are submitted within the legal timeframe and with the necessary documentation;
- Monitoring the progress of processes with regulatory bodies;
- Updating the registrationdata of Ceva Brazil subsidiaries and their technical managers with thecorrespondingbodies;
- Preparing and requesting the necessary documents from official bodies for the import and export of veterinary products, submitting the requested documents and makingthem available to the requesting areas;
- Controlling, preparing, and organizing production, product import and export maps; maps ofofficially controlled products and substances (periodic reports), in compliance with current regulations, sharing activitieswith other areas of thecompany;
- Assisting in the execution of product registration processes, adjustments, and updates with MAPA;
- Prepare and control the documentation for the collection of vaccines for official control by MAPA and monitor the official results, and ensure that they are in accordance with current regulations and madeavailable to the various sectors within the established timeframe;
- Assisting in meeting MAPA requirements, participating in the review and assemblyof dossiers and response processes;
- Checking the wording on packaging,advertising leaflets and technical bulletins, ensuring that they comply with documents approved by MAPA (approved forms, technical reports, etc.);
- Checking documents from the Quality Assurance and Production areas, such as manufacturing instructions, specifications, and Certificates of Analysis, ensuring their conformity with documents approved by MAPA (licenses, approved forms, technical reports, among others);
- Assisting in the assembly and organization of product dossiers for subsequent official submission;
- Updating outsourcing contracts(contractor and contracted), ensuringthat they are up to date with therelevant bodies;
- Support Ceva's subsidiaries in the regulatory area by providing relevant documentation for veterinaryproducts produced in Brazil and other information required;
- Assisting in the sharing of documents for products manufactured in Brazil and exported to other countries.
**Your profile**:
- Complete university degree or studying Veterinary Medicine
- National legislation on veterinary establishments and products
- Electronic submission systems of the relevant bodies, mainly MAPA
- Knowledge of Good Manufacturing Practices (National and International)
- Advanced English

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