Bernadett Samu

Coordination and management of product and process information to ensure development of efficient and consistent full-scale manufacturing processes.

The key component of this position focused on product development activities of parenteral products with the use of QbD elements. The development activities involved optimisation of formulation parameters ensuring that the set specifications were met, evaluation of primary packaging and technology applications, interpretation and adaptation of scientific data.

This position was focused on preparing formulations such as in vivo solutions, in vitro solutions/suspensions, capsules, creams, intranasal formulations, diets and inhalation blends for Safety Assessment studies in Pre-Clinical Development; conducting solubility, stability and vehicle assessment studies for candidate drugs.