Bruna Dias

Quality Assurance & Regulatory Affairs Specialist at Werfen

Bruna Dias is a Quality Assurance & Regulatory Affairs Specialist at Werfen since January 2024, focusing on the management and approval of medical and in vitro diagnostic devices, quality complaint management, and supporting commercial and public procurement departments. Previously, Bruna served as the Quality Assurance & Regulatory Affairs Manager at HR Hospitalar, Lda, from May 2021 to January 2024, overseeing regulatory compliance for various health products and ensuring the implementation of good distribution practices. Bruna's experience also includes roles in training moderation and community pharmacy, along with internships in clinical analysis, highlighting a strong background in regulatory affairs and quality assurance. Educational qualifications include a postgraduate course in Advanced Cosmetology and specialization in Regulatory Affairs & Technical Direction, alongside a Master's degree in Pharmaceutical Sciences from Universidade de Coimbra.

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