As the (Sr.) Qualified Person you will focus on the batch certification and release of pharmaceutical products in accordance with the Marketing Authorisation/IMPD and in accordance with current EU-Directives. Part of the role entails to investigate in close collaboration with the Deviations Specialist and approve/finalise the deviation(s), approval of Change Controls and being the focal point of contact with regulatory authorities (IGZ, Farmatec, PEI) to maintain the compliance status. Moreover, you will participate in R&D Project teams as QA-representative, focus on approval and execution, including follow-up of internal – and external (supplier) audits and support quality-based decision processes. You will also participate in developing and training QA-Officers and actively support a climate for continuous improvement, take care of maintenance of the Quality Management Systems: Auditing, Deviations and Product Quality Review.