Together with the team from Change Control Management, you will evaluate and facilitate changes that are due to be introduced in the production and testing of our medicinal products, for example variations to the manufacturing process or to analytical methods. For this, you will collate information and define, jointly with the involved areas Manufacturing, Quality Control and Regulatory Affairs, the activities that are necessary for introducing the change. In this way, you will gain an overview of the GMP and regulatory requirements as well as the many different aspects of variations.
