Regulatory Affairs Jr. Analyst - Sao Paulo, Brasil - CEVA Animal Health, LLC

CEVA Animal Health, LLC
CEVA Animal Health, LLC
Empresa verificada
Sao Paulo, Brasil

há 1 semana

Ana Silva

Postado por:

Ana Silva

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Descrição

Regulatory Affairs Jr. 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.


Your missions:

Maintain the filing of regulatory documents up to date and available for consultation in the department's database, as well as their physical layout;

  • Assist in maintaining product and establishment licenses before regulatory bodies;
  • Carry out the organization and assembly of regulatory processes for subsequent review by managers;
  • Collaborate in the execution of product registration processes, adjustments and updates with MAPA;
  • Help in meeting requirements with MAPA, participating in the review and assembly of dossiers and response processes;
  • Check the wording on packaging, marketing leaflets, technical bulletins, ensuring their compliance with documents approved by MAPA (approved forms, technical report, etc.).
  • Provide technical documents such as copies of licenses, copies of approved forms, among others, requested by internal and external areas;
  • Prepare necessary documents for the import and export of veterinary products, in order to collaborate with the processes to be submitted to regulatory bodies;
  • Keep product technical information up to date in corporate and external databases and corresponding compendiums

Your profile:


  • Completed higher education or studying Veterinary Medicine or Pharmacy
  • Previous contact with scientific research or bibliographic reviews
  • Intermediary English

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