You’re an important part of our future. Hopefully, we're also a part of yours! At B. Braun, we protect and improve the health of people worldwide. This is also our vision for research and development. You see complexity as an opportunity – and quality and sustainability are important criteria for your work. We would like to work with you on tomorrow’s solutions. That’s how we work to create sustainable healthcare – locally, in regions, countries and worldwide. Together. That's Sharing Expertise.Reference Code DE HB 2324-91350Within the Quality Management of the Hospital Care division, we are looking for a Head of (f/m/d) Business Process Management & Pharmacovigilance Tools within the Global Pharmacovigilance & Patient Safety (GPVS) department at our Group headquarters in Melsungen as soon as possible. The GPVS department documents and evaluates reports of drug risks that become known and coordinates the necessary measures in accordance with Good Pharmacovigilance Practice (GVP). As Head of (f/m/d) Business Process Management & Pharmacovigilance Tools, you will manage the team responsible for maintaining and improving pharmacovigilance processes and the applications (e.g. ICSR database, Signal and Risk Management application). You will interact within the function's global network, for example with our Shared Service Centre based in Romania and B. Braun’s affiliates worldwide.Duties and responsibilitiesYou lead and develop a team of seven technofunctional and subject matter expertsYou implement, maintain, and improve pharmacovigilance processes in close collaboration with the business teams and related departmentsYou implement, maintain, and improve applications owned by pharmacovigilanceYou maintain good relations and negotiate with external partnersYou oversee the global processing of pharmacovigilance-related deviations and corrective and preventative action (CAPA)Professional competenciesYou have successfully completed a master’s degree or equivalent in natural sciences with a bio-medical background (e.g. pharmaceutical sciences)You possess multiple years of professional experience in pharmacovigilance processesYou are characterized by a high technical affinity for process simplification and automationsYou are familiar with project management Understanding electronic processing and reporting of Individual Case Safety Reports, short CSRs, (such as E2B, MedDRA, etc.) comes easy for youYour profile is completed by excellent written and spoken English skillsPersonal competenciesYou are a natural networker and can build sustainable partnerships You enjoy initiating and supporting ideas, innovations and change processesYou appreciate and include different perspectivesWhat we offerBecome part of a corporate culture that actively promotes constructive exchanges between colleagues, customers and partners. Work with us to improve people's lives in the long term. We can offer you interesting, varied tasks and excellent opportunities for advancement, as well as an attractive salary with extensive benefits, all within a dynamic family-owned company.