Nicole Marty

Take care of all drug regulatory affairs matters, act business-oriented and timely as an interface between global Regulatory Affairs departments and Swissmedic in order to obtain new, on-time marketing authorizations, support new product launches and ensure regulatory compliance.

Responsible for the independent design, construction and testing of optimized innovative antibody fragments and bivalent/bispecific antibodies with drug-like properties via rational and evolutionary approaches; responsible for the development of the phage display protein engineering platform via improvement of the current technology and implementation of new complementary techniques and application for current projects of the DA

As part of the quality control department I was responsible for the support of the drug stability analysis, the Preparation of Stabilitymasterplans, the coordination of Analysis samples ant the data control and data reconciliation according GMP guidelines

Biochemistry, Social- and communication psychology