Cell Chain Manager

For 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).

Job Title: Cell Chain Manager

Duration: 12 months

Location: Basel

Workload: 100%

Leads the system support (master data management, process support, testing, validation, documentation and training) regionally for the efficient, effective operations of Cell Chain and for all internal and external stakeholders.

• Lead the Cell Chain support for user management, master data management and change control.
• Build user adoption and expertise in utilizing Cell Chain to enhance customer engagement and supply chain performance.
• Develop and implement Cell Chain continuous improvement opportunities.
• Manage country launches, including corresponding site set‑ups and user account set‑ups in support of all commercial and clinical launches.
• Implement the medium and long term operational strategy for Cell Chain with a focus on:
  • Scaling the business – Customer engagement, New Clinical Trials, Commercial PedALL, DLBCL, Country Launches, New Treatment Sites, New Manufacturing Sites.
  • Enhancing supply chain performance
  • Maintaining COI
• Tighter integration and engagement with Cell Chain business partners (Treating Sites, Aph Centers, Cell Labs, Service Providers).
• Streamlining and maintaining Computer System Validation.
• Mobile platform strategy.
• Support Cell Chain system releases managing PQ testing, change control impacts, user training.
• Improve the System Evolution and Lifecycle processes for Cell Chain.

• University Degree in supply chain management or operations. The following certifications a plus: APICS CSCP, CPIM English.
• Deep supply chain system experience with ERP and CRM applications. Deep experience with GxP Validated systems. International experience a plus.
• Significant 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).
• ERP Master Data set‑up subject matter expert.
• Experience in a cGMP manufacturing environment. Deep experience in supporting 21
  
  CFR Part 11 Computer System Validation and HIPAA regulations.
• Broad general business knowledge with experience collaborating with and supporting multiple functional areas, such as commercial, finance, quality, regulatory, compliance, IT and manufacturing.
• FDA Audit participation experience.

We are looking forward to receiving your CV for review. Kindly only apply if you have a valid Swiss work permit or EU citizenship.