Introduction letter
Envie uma proposta de trabalho diretamente para este candidato
Pharmaceutical professional, have been working for more than 20 years in the regulatory area of medicines. I started my experience in this segment in 2000 as a technical consultant at the General Management of Medicine - GGMED/ANVISA. There I developed my regulatory skills that were improved with a postgraduate degree in Health Surveillance and another in Public Health. With the entry of the technicians I was assigned to train them and in this process I made friends that last until today.
My first experience in the pharmaceutical industry was as a Government Relations Manager at Abbott. Later I assumed the posi4on of Regulatory Affairs and Quality Assurance Manager at Genzyme, which was acquired by Sanofi. After 4 years I started in Pfizer's consumer division as Senior Manager of Regulatory Affairs.
Where I had a great opportunity for development, including receiving an award due to the successful implementa4on of a strategic regulatory solu4on. This division was negotiated in a joint venture with GSK.
After the consolidation of Join Venture, the company was restructured and I was terminated in this process. I started in the same year at Dr. Reddys, taking over the regulatory area along with the areas of Pharmacovigilance and Quality Assurance
Throughout this trajectory, I led committed teams that helped me achieve great goals, I cooperated with my managers to achieve the proposed goals and oUen exceed them. I witnessed the changes in ANVISA's regulatory framework and learned how to adapt products and companies to the requirements of natioonal and internatioonal regulatory bodies.
I am currently looking for the opportunity to participate in challenging projects where I can cooperate with my exper4se in regulatory strategy and team leadership and contribute to the success of the institution with which I will work.