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    Clinical Supply Program Lead - Amman, الأردن - AstraZeneca

    AstraZeneca
    AstraZeneca Amman, الأردن

    منذ 18 دقيقة

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    وصف
    • 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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