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Senior Manager, Supply Chain Operations

vor 2 Monaten


Basel, Basel-Stadt, Schweiz BeiGene Vollzeit
About the Role

We are seeking a highly experienced Senior Manager, Supply Chain Operations to join our team at BeiGene. As a key member of our Supply Chain organization, you will be responsible for managing our global Contract Manufacturing partnerships, driving productivity through strategic initiatives, and ensuring that innovation, manufacturing performance, cost objectives, and quality goals are met or exceeded at Contract Manufacturers.

Key Responsibilities
  • Manage all aspects of global Contract Manufacturing partnerships, driving productivity through strategic initiatives with Contract Manufacturers (CMO)
  • Partner with Quality, CMC, Procurement to ensure that innovation, manufacturing performance, cost objectives, and quality goals are met or exceeded at CMOs
  • Develop and maintain CMO management governance structure, communication matrix, standard templates (playbook) to properly address supply chain and quality issues with timely root cause and corrective actions
  • Coordinate with Procurement, Quality, and other internal departments to cross-functionally resolve elevated issues
  • Develop and maintain KPIs for CMO
  • Oversee monthly actual-to-budget cost variances, identify root cause, and drive cost improvements
  • Promote and drive contract manufacturing production efficiency
  • Support Procurement to negotiate CMO contracts, amendments, and renewals, aligning with the business strategies
  • Project management of multiple complex project teams for commercial and operational excellence
  • Manage new product and new market launch activities related to supply chain along with other key functions (Commercial, S&OP, Manufacturing, SC Planning, Logistics, Quality, MDM, and commercial Artwork services) and track progress for on-time launch
  • Key business partner in the project core team monitoring key milestone progress against the plan and communicating achievements or deviations to launch plans
  • Ensure that identified continuous improvement opportunities in the overall launch processes
  • Work closely with key business partners in Tech Ops, Regulatory; Supply Chain; Commercial; Quality to establish clear processes and deliverables
Requirements
  • Bachelor's degree in a scientific field
  • Minimum 7+ years' experience within biopharmaceutical/pharmaceutical CMC development, GMP, and regulatory requirements
  • Experience in pharmaceutical project management
  • Strong experience in Project Management Office (PMO) processes, creating templates, and training materials
  • Excellent organizational skills, capable of setting priorities and managing high workload
  • Strong communication skills written and verbal, including oral presentation skills
  • Ability to interact with multiple layers of the organization with demonstrated success initiating change and influencing at all levels
  • Understands comprehensive global pharmaceutical regulatory requirements (e.g. GMP, GDP)
  • Strong analytical, problem-solving, and communication skills
  • Strong collaboration and excellent team skills to be successful in cross-functional and multi-cultural teams
  • Computer skills: In-depth knowledge and skill with Microsoft Project, Excel, PowerPoint, Word, Visio, and other reporting/tracking tools