What I do at MMV:
I manage all quality aspects from discovery to products being registered in the different countries around the globe (GLP, GMP, GcLP, GCP and GVP).
Why I work at MMV:
I consider it a great achievement to work for an organization such as MMV. As a Swiss with Ghanaian origin, I have always been interested in contributing to the work being done in malaria endemic countries. MMV’s values and objectives are totally in line with mine. Moreover, working in a multicultural environment with experts who have such diverse backgrounds is very rewarding. I am proud to contribute my expertise and to help bring high quality and affordable medicines to those in need.
More about me:
Before joining MMV, I worked in a Contract Manufacturing Organization as a co-qualified person (quality & regulatory) for 5 years. I was responsible of all the documentation, the quality systems and all regulatory aspects. Prior to that, I gained experience in Medtech, as I participated in the implementation of the Quality system of a start-up. I have a Master’s degree in molecular and biological chemistry from the EPFL. After attending several trainings on different aspects of Quality, I completed a CAS in Management of Pharma, Biotech and Medtech Ventures.
Ask me about:
The Do’s and Don’ts related to Quality … and travelling as well as cooking.