Quality & Regulatory Affairs | Medical Devices - Viseu
Apenas para membros registrados Viseu, Portugal
há 2 semanas
Job summary
We are looking to strengthen our team with a Quality & Regulatory Affairs profile. The role will implement and maintain the Quality Management System in a manufacturing environment and ensure compliance with regulatory requirements.Responsibilities
- Implement, maintain and continuously improve the Quality Management System in a manufacturing environment.
- Prepare and maintain MDR technical documentation (technical files).
- Support certification processes and regulatory compliance activities.
Descrição do trabalho
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