Senior Manager/Director Supply Chain Management Biopharmaceuticals

vor 2 Wochen

Bad Homburg vor der Höhe, Hessen, Deutschland Fresenius Kabi Vollzeit 90.000 € - 120.000 € pro Jahr

As a (Senior) Manager/Director Supply Chain Management Biopharmaceuticals (m/f/d), it is your main responsibility to ensure timely product launches and the continuous supply of biosimilar products to the markets.

Your Assignment

  • Analyze global demand vs. supply for one or more biosimilar molecules
  • Provide transparency on demand vs. supply to enable cross-functional alignment and management decisions
  • Prepare and participate in S&OP cycles and drive demand, inventory, and supply analysis
  • Forecast Drug Substance and Drug Product demand based on Finished Product sales forecasts (horizon 36 months)
  • Manage ordering process, and production planning, and coordination with suppliers for Drug Substance (DS), Drug Product (DP), and Finished Products (FP)
  • Oversee inventory at all supply chain levels (DS, DP, FP)
  • Lead supply launch readiness and ensure cross-functional alignment and adherence to timelines
  • Support Tech Transfer projects and Business Development initiatives
  • Participate in SCM projects together with the Global SCM group

Your Profile

  • Degree in Business Administration, Industrial Engineering, Supply Chain Management or similar
  • Min. 5 years of experience in number-driven environments (e.g., finance, supply chain, consulting or similar)
  • Strong knowledge of end-to-end supply chain processes, including external manufacturing and launch management in the biopharmaceutical industry
  • Track record in setting up processes, tools and structures and project management experience
  • Very proficient use of Excel and ability to build simple to advanced models to run analysis over several manufacturing steps
  • Experience in S&OP / IBP and S&OE processes and proficient use of SAP ERP and SAP IBP is an advantage
  • Track record in setting up processes, tools and structures and project management experience
  • Knowledge of (bio)pharmaceutical manufacturing processes, GMP, regulatory requirements, QA and QC is plus
  • Continuous improvement mindset and/or certificate(s) such as Lean Six Sigma Greenbelt, Blackbelt, etc. is a plus
  • Excellent organizational, team and time management skills
  • Critical thinking, solution oriented and proactive work style
  • Fluent in English, with additional language skills (German or French) as a plus

Please submit your application including a cover letter, your CV and copies of relevant certificates or references.

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