Your role in our teamYou are responsible for an international team of motivated employees.You are responsible for the quality of all PAS X MES versions within the PAS X product development team.You are responsible for the informal (exploratory testing) and formal testing (FAT) and its automation of PAS X MES within the PAS X product development team.You will shape the future processes to increase the quality of PAS X MES and to support a continuous integration / evergreen process.You will develop, implement, and maintain a robust QA strategy aligned with agile methodologies, specifically Scrum.Oversee all aspects of quality assurance including test planning, automation, execution, and reporting.Ensure the timely and effective delivery of PAS X MES product patches, hotfixes, and service packs.You will increase the level of test automation to ensure a right first time approach to quality.Together with the other PAS X product HoDs, you further develop the collaboration in product development and thus set the course for a successful future of or product PAS XYou optimize the processes for the creation and delivery of product development.Monitor and report on key quality metrics and drive continuous improvement initiatives.Ensure compliance with GMP regulations and other relevant industry standards.Mentor and develop QA team members, fostering a culture of quality and continuous improvement.Your profileYou enjoy creating a positive and productive working environment for your staff.You enjoy working with international and intercultural teams.You are highly motivated to develop yourself and your employees.You have a positive attitude towards change and an interest in helping to shape it.You enjoy playing a central role in shaping Korber Pharma Software''s path to becoming a product company.You have a strong sense of mission and the ability to achieve it together with the team.You have deep understanding of QA methodologies, best practices, and industry standards.You have experience in developing and implementing QA strategies and processes.You are familiar with the pharmaceutical industry and understanding of regulatory requirements (e.g., FDA, GMP).You could manage multiple projects simultaneously, ensuring timely delivery and quality standards.You have strong analytical abilities to identify, diagnose, and resolve quality issues.You have experience with agile methodologies and tools (e.g., Scrum, Kanban).You have very good written and spoken German and English skills.Experience with Pharmaceutical Manufacturing Execution Systems (MES) is a plus.Your benefitsBe part oftheinternationalMESworld market leader inpharmaFlexible working hours,hybrid workGlobaldevelopment prospects,group wideperspectives,and further training opportunities32 daysof vacation per yearAnnual salary reviewandoccasion relatedspecial paymentsAttractive workplace with modern equipmentFlathierarchies andshortdistances, andinformal corporate cultureIncreased em