Clinical Supply Program Lead
Posted on :
25-04-2024
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1 Vacancy
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Job Description
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.
Employment Type
Full Time
Department / Functional Area
Key Skills
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