Ph3Role Purpose /h3 pThe Supply Chain Manager (SCM) is responsible for Demand and Supply Planning from Clinical Finished Good (CFG) to Drug Substance (DS) and Booklet labels, ensuring demand fulfillment for assigned projects. The SCM acts as a key contributor to the Clinical Supply Operations Planning (CSOP) process in TRD/GCS, provides transparency on supply constraints and manages related aspects accordingly within TRD. The role has operational end‑to‑end responsibility for assigned activity, leads and manages all project and local network activities, and participates in cross‑functional teams. /p h3Summary /h3 pLocation: Basel, Switzerland, onsite. /p h3Major Accountabilities /h3 ul liHarmonises the supply strategy within GCS and contributes to the supply strategy of CHAD/PHAD/Biologics. /li liParticipates in the GPMM along with the CSPL and CTSM ensuring alignment between demand and supply. /li liEnsures demand fulfillment and coverage of supply and regulatory aspects by contributing to the GCS agenda at TRD Sub team CMC meeting, representing GCS at TRD Sub‑team on supply chain aspects. /li liActively contributes to the portfolio manufacturing schedule alignment (from DS to CFG), defines the most cost‑efficient ordering levels from CFG to DS, minimises waste and allows flexibility to accommodate demand variability. /li liDrives long‑term demand and capacity planning (LTDCP) coordinating with CSPL, DPPL, DSPL and TPL, and adheres to SCM KPIs including participation in SPE for projects and units. /li liProactively manages and adheres to functional performance indicators with a focus on supply planning excellence. /li liData and digital savviness in SC domain; manages ordering and master data requirements in SAP within the scope of the role. /li liAdapts and implements Rapid Response (Maestro) for portfolio supply demand planning, network design and scenario building. /li liEstablishes the supply chain design in alliance with Funds Flow, Customs Trade Compliance and TRD sub‑team for portfolio. /li liDrives the change control strategy for clinical supplies from GCS perspective. /li liProvides impact assessment on clinical supplies and contributes to regulatory submission strategy. /li liIntegrates comparator supply strategy into TRD procurement, blinding release planning. /li /ul h3Minimum Requirements /h3 ul liDegree in science, engineering or equivalent. /li liFluent English. /li liMore than 5 years of practical experience in the chemical/pharmaceutical industry or more than 3 years in a relevant field. /li liGood expertise in related field. /li liGood knowledge of the drug development process. /li liBasic project management, good organisation and planning skills. /li liKnowledge of relevant regulations (e.g., GMP, HSE, etc.) and Novartis specific standards. /li liDemonstrates problem‑solving and idea‑generation skills. /li liGood presentation skills. /li liIntermediate leadership skills. /li liVery good communication, negotiation and interpersonal skills. Ability to work in interdisciplinary teams. /li /ul h3Commitment to Diversity and Inclusion /h3 pNovartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. /p h3Accessibility and Accommodation /h3 pNovartis is committed to working with and providing reasonable accommodation to all individuals. /p /p #J-18808-Ljbffr