Analista de Operações Regulatorias Nível Sênior - Divisão de Dispositivos Médicos (MD)

Serve as a regulatory representative, reviewing and analyzing GTS blocked orders, and coordinate activities to resolve issues. Maintain a basic understanding of product lines and organize product information for internal procedures, reporting, quality plans, and audit needs. Understand and utilize Windchill and other business systems for change control, documentation control, and other Regulatory Affairs interactions.

Minimum of 3 – 4 years experience in Regulatory Affairs, Regulatory Operations, Quality Assurance or related area in Medical Device industry. Bachelor's degree completed. Fluent in Portuguese and English, with strong verbal and written communication skills. Experience with completing tasks in ERP system, SAP preferred.

Career development with an international company where you can grow the career you dream of. Benefits such as Medical and Dental Assistance, Life Insurance, Private Pension Plan, Medication Subsidy, Discount on Abbott stock purchases, among others.