-This role utilizes chemistry laboratory skills to test and measure product or materials while ensuring that analysis is performed according to established Standard Operating Procedures (SOPs), Analytical Methods & current Compendia.
About the RoleMajor accountabilities: 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 / special case scenarios related to Novartis products within 24 hours of receipt -Distribution of marketing samples (where applicable)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 planSound technical & scientific knowledge of pharmaceutical/ chemical.Working experience in Laboratory environment in the Pharmaceutical.analytics/QC/ equivalent.Skills: Dealing With Ambiguity.Decision Making Skills.Gxp.Industry Standards.Laboratory Equipment.Laboratory Excellence.Quality Control (Qc) Testing.Quality Control Sampling.Technological Expertise.Total Quality Management.Languages : 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? https://www.novartis.com/about/strategy/people-and-culture
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