Your primary responsibility will be to lead the MS&T (Manufacturing Science & Technology) department. You will be in charge of process development, improvement and validation for all products, which are produced at the manufacturing sites in Ulm and Weiler. This includes technologies for oral solid dosage forms, sterile, semisolid and liquid dosage forms. You will be responsible for planning and realization of AOP budget, capacity, trainings and investments within MS&T.
You will lead and coordinate various initiatives within MS&T, including projects for product robustness on site as well as global, multinational, cross-functional projects. Additionally you will assure implementation of GMP requirements according to guidelines from authorities and internal from Teva. Furthermore, you will be in charge of transfer and implementation of new products from local and global R&D as well as from external contract development labs. You will act as a main point of contact for local authorities, quality investigations and all product and technology related questions.