PpFor our client, a leading global medicine company consistently ranking among the world’s top companies investing in research and development with products reaching nearly 1 billion people globally we are currently recruiting a Cell Chain Manager (m/f). /p pbJob Title: /b Cell Chain Manager /p pbDuration: /b 12 months /p pbLocation: /b Basel /p pbWorkload: /b 100% /p h3Job Description /h3 pLeads the system support (master data management, process support, testing, validation, documentation and training) regionally for the efficient, effective operations of CellChain and for all internal and external stakeholders. /p h3Major Accountabilities /h3 ul liLead the CellChain support for user management, master data management and change control. /li liBuild user adoption and expertise in utilizing CellChain to enhance customer engagement and supply chain performance. /li liDevelop and implement CellChain continuous improvement opportunities. /li liManage country launches, including corresponding site set‑ups and user account set‑ups in support of all commercial and clinical launches. /li liImplement the medium and long term operational strategy for CellChain with a focus on: ul liScaling the business – Customer engagement, New Clinical Trials, Commercial PedALL, DLBCL, Country Launches, New Treatment Sites, New Manufacturing Sites. /li liEnhancing supply chain performance /li liMaintaining COI /li /ul /li liTighter integration and engagement with CellChain business partners (Treating Sites, Aph Centers, Cell Labs, Service Providers). /li liStreamlining and maintaining Computer System Validation. /li liMobile platform strategy. /li liSupport CellChain system releases managing PQ testing, change control impacts, user training. /li liImprove the System Evolution and Lifecycle processes for CellChain. /li /ul h3Requirements /h3 ul liUniversity Degree in supply chain management or operations. The following certifications a plus: APICS CSCP, CPIM English. /li liDeep supply chain system experience with ERP and CRM applications. Deep experience with GxP Validated systems. International experience a plus. /li liSignificant project management experience, particularly with running complex multi‑functional technology projects that tie technology solutions to business operations and internal and external stakeholders. Program Management experience a plus. Experience in supporting tools (Microsoft Project). /li liERP Master Data set‑up subject matter expert. /li liExperience in a cGMP manufacturing environment. Deep experience in supporting 21CFR Part 11 Computer System Validation and HIPAA regulations. /li liBroad general business knowledge with experience collaborating with and supporting multiple functional areas, such as commercial, finance, quality, regulatory, compliance, IT and manufacturing. /li liFDA Audit participation experience. /li /ul pWe are looking forward to receiving your CV for review. Kindly only apply if you have a valid Swiss work permit or EU citizenship. /p /p #J-18808-Ljbffr