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Analista de Assuntos Regulatórios Pleno

CEVA SANTE ANIMALE

Paulínia

Presencial

BRL 30.000 - 60.000

Tempo integral

Há 30+ dias

Melhora as tuas possibilidades de ir a entrevistas

Cria um currículo adaptado à oferta de emprego para teres uma taxa de sucesso superior.

Resumo da oferta

Uma empresa global líder em saúde animal busca um Analista de Assuntos Regulatórios apaixonado e dedicado. Nesta função, você será responsável por preparar e controlar a documentação necessária para processos regulatórios, garantindo conformidade com as exigências legais. Você terá a oportunidade de trabalhar em um ambiente dinâmico e colaborativo, onde suas contribuições são valorizadas e fazem a diferença na saúde e bem-estar dos animais. Se você é um profissional com formação em Medicina Veterinária e deseja fazer parte de uma equipe que se preocupa com a saúde do planeta, esta posição é para você.

Qualificações

  • Formação em Medicina Veterinária é essencial para o cargo.
  • Conhecimento da legislação nacional sobre produtos veterinários é necessário.

Responsabilidades

  • Preparar documentação para processos regulatórios junto a autoridades competentes.
  • Monitorar o progresso de processos com autoridades regulatórias.

Conhecimentos

Veterinary Medicine
Knowledge of national legislation
Electronic submission systems
Good Manufacturing Practices
Advanced English proficiency

Formação académica

Degree in Veterinary Medicine

Descrição da oferta de emprego

Regulatory Affair PL. Analyst

The success of a company depends on the passionate people we partner with.

Together, let's share our talents.

As a global leader in animal health, Ceva Animal Health believes our success is linked to our passionate people researching, developing, producing and supplying innovative health solutions for all animals, which contributes to the future of our diverse planet.

We are committed to ensuring the highest possible level of care and well-being for farm animals (poultry, pigs, ruminants), companion animals (dogs and cats) and wildlife.

Indeed, Our “Together, Beyond Animal Health” vision emphasizes that the health and wellbeing of people, animals and our planet are totally interlinked. More than ever, Ceva is committed to a "One Health" approach.

As part of our “Diversity, Equity and Inclusion” policy, Ceva Animal Heath is committed to the employment of people with disabilities and will make reasonable accommodations throughout the interview process to ensure an inclusive and accessible experience for all applicants. To request an accommodation, please contact a member of the Ceva Talent Acquisition team.

Your missions:

  1. Prepare documentation for regulatory processes to be submitted to regulatory authorities;
  2. Handle the renewal of product and establishment licenses with relevant authorities (MAPA, Anvisa, professional councils, among others), ensuring the submission of processes within legal deadlines and with the required documentation;
  3. Monitor the progress of processes with regulatory authorities;
  4. Update the registration data of Ceva Brasil branches and their technical representatives with the relevant authorities;
  5. Prepare and request necessary documents from official authorities for the importation of veterinary products, submitting the requested documents and making them available to requesting areas;
  6. Assist in the execution of product registration processes, adjustments, and updates with MAPA;
  7. Prepare and control documentation for the collection of vaccines for official control by MAPA, monitor official results, ensure compliance with current regulations, and make them available to various departments within the established timeframe;
  8. Assist in meeting requirements with MAPA by participating in the review and preparation of dossiers and response processes;
  9. Verify the labeling of packaging, promotional brochures, and technical bulletins to ensure compliance with documents approved by MAPA (approved prints, technical reports, etc.);
  10. Ensure the compliance of documents approved by MAPA (licenses, approved prints, technical reports, among others);
  11. Assist in the preparation and organization of product dossiers for subsequent official submission;
  12. Update outsourcing contracts (contractor and contracted parties), ensuring their compliance with relevant authorities;
  13. Support Ceva branches in regulatory matters by providing relevant documentation for veterinary products manufactured in Brazil and other requested information.

Your profile:

  • Completed or ongoing degree in Veterinary Medicine
  • Knowledge of national legislation related to veterinary establishments and products
  • Familiarity with electronic submission systems of relevant authorities, especially MAPA
  • Knowledge of Good Manufacturing Practices (national and international)
  • Advanced English proficiency
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