Ph3Responsibilities /h3 pTaking care of the quality management software as system administrator. /p ul liSupport and train users. /li liImprove and update processes including relevant SOPs and documents. /li liHarmonize processes. /li liLead projects. /li liImplement additional modules and functionalities within the quality management software. /li /ul h3Qualifications /h3 ul liBackground in analytical chemistry, biochemistry, or life science. /li liExperience in the analytical‑pharmaceutical environment, preferably in QA. /li liSkills to solve problems and build good relationships with stakeholders. /li liGood interpersonal skills and teamwork spirit. /li liAbility to collaborate in a dynamic, cross‑functional matrix environment. /li liAbility to lead projects between sites and work independently. /li liBroad knowledge and proven experience of the regulatory framework in the GMP environment (ICH, FDA, USP, Ph.). /li liSolid background in data integrity and computerized systems risk assessment and project support. /li liExperience as system administrator or deeper IT knowledge is an asset. /li liFluency in English and German is a plus and required. /li /ul /p #J-18808-Ljbffr