Clinical Supply Program Lead

3 weeks ago


Amman, Jordan AstraZeneca Full time

  • Responsibilities will include:

  • Influencing the design phase with relevant experts to drive an optimized supply chain design with respect to quality, risk and cost for the business
  • Working in conjunction with the Supply Chain planner to guarantee: Balancing Short to Mid-term Supply and Demand, Inventory Management, input into D&OP Process, planning Excellence Process Requirements, SS Master Data Management
  • Overall endorsement of the supply plan
  • Maintaining appropriate information for supply activities in PLANIT in line with RBU.
  • Ensuring ongoing supply through transition from development sources to commercial sources of manufacture.
  • Managing change in demand and supply, resolve issues, escalating when appropriate.
  • Understanding and acting according to GxP and understanding the impact it has on supply chain activities.
  • Ensuring timely delivery of information to meet internal and external regulatory and legal requirements.
  • Working with CSSLs to resolve issues, share standard processes and continually develop competence.
  • Promoting supply chain practice in PT&D and interfacing functions
  • Being responsible for introducing innovation into the Supply chain ensuring a culture of continuous improvement.
  • Taking lead in motivating others within the function and communicating the Supply Chain strategies.
  • Taking responsibility for handling issues and making complex trade-offs with both internal and external partners. This will require well developed conceptual and analytical thinking to make complex judgements and deliver innovative solutions.
  • Acting as a sponsor to support and manage the implementation of supply chain change and be the 1st point of contract for Senior Stakeholders within the organizations.

  • Essential Skills/Experience:

  • Minimum education BSc or equivalent in a relevant subject area
  • In-depth knowledge of supply chains and drug development process.
  • In-depth knowledge of Clinical Development processes relevant to investigational products.
  • Awareness of GXP Standards within a Clinical environment.
  • Demand management and forecasting experience.
  • In-depth experience of project management and influencing and leading business partner relationships.
  • Proficient IT skills with an ability to adapt and operate in multiple systems.
  • Strong influencing, negotiating, and problem-solving skills across geographical and cultural boundaries.

  • Desirable Skills/Experience:

  • Working knowledge of the Clinical Trial Directive and global regulatory environment impacting the provision of investigational products.

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