Summary ~ Diese Rolle nutzt chemische Laborfähigkeiten, um Produkte oder Materialien zu testen und zu messen und gleichzeitig sicherzustellen, dass die Analyse gemäß etablierten Standard Operating Procedures (SOPs), Analytischen Methoden und aktuellen Kompendien durchgeführt wird. About the Role Sample storage and management -Analytical testing/documentation of drug product / finished product / complaints / stability / packaging material samples to GxP standards Stability -Testing/Sample storage and management. Analytical documentation of stability samples to GxP standards -Reporting of technical complaints / adverse events. Key performance indicators: Orders are processed correctly and quickly. No waiting times due to wrong or delayed order. Deadline adherence rate: orders completed on time, all missed deadlines reported in good time, the shortest possible lead time -Ensure constant readiness for inspection, no critical complaints from superiors and inspectors -Consistently follow the GMP and GSU guidelines, as well as the SOPs, no critical irregularities -Finding and implementing optimization options to reduce costs -Completed training plan Minimum Requirements: Work Experience: Working experience in Laboratory environment in the Pharmaceutical. Sound technical & scientific knowledge of pharmaceutical/ chemical. industry. analytics/QC/ equivalent. Language: Englisch Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: is external) Benefits and Rewards: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: