Clinical Supply Program Lead
AstraZeneca AB / Biomedicinjobb / Göteborg
2023-03-28
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hela Sverige AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialisation of prescription medicines for some of the world's most serious disease. But we're more than one of the world's leading pharmaceutical companies.
In Pharmaceutical Technology and Development (PT&D) at AstraZeneca we are the bridge which turns forward-thinking science into actual medicines that help millions of people around the world. We work across the entire value chain, crafting and delivering active ingredients, formulations and devices required to support new medicines - from supplies for use in early toxicology studies and clinical trials to developing the technology to ensure drugs can be scaled up for commercial manufacture.
We have an exciting opportunity for a Clinical Supply Program Lead to join are fantastic team.
This is a key role within Global Clinical Supply Chain where the role holder is accountable for the end-to-end clinical supply chain of products being delivered to our clinical trials. This includes having specific responsibility for the long-term strategy of the clinical supply chain.
What you'll do
In this role, you will Lead the Supply Chain Team (SCT) which is accountable for developing and maintaining the supply plan for a programme. You will lead a matrix multi-functional team to drive strategy and to manage supply chain performance through key performance indicators. You will be a key facilitator of cross-functional collaboration working across different organizations and will represent R&D Supply Chain at PT&D and Global project teams.
Your accountabilities will include but not be limited to:
* Influencing the design phase with relevant experts to drive optimized design, managing quality, risk and cost for the business
* Monitoring the performance of the supply chain and optimizing for higher volume/later phases of the project, balancing speed, quality and cost with respect to the agreed level of risk.
* Understanding and acting according to GxP and the overall impacts on supply chain activities.
* Driving overall endorsement of the supply plan
* Being accountable for a significant budget for supply activities and materials for the project.
* Maintaining appropriate information for supply activities in PLANIT on an ongoing basis and in line with RBU.
* Ensuring ongoing supply through transition from development to commercial sources of supply.
* 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.
* Managing change in demand and supply, resolving issues and escalating when appropriate.
* Ensuring timely delivery of information to meet internal and external regulatory and legal requirements.
* Being responsible for introducing innovation into the Supply chain ensuring a culture of continuous improvement is encouraged and managed.
* Taking responsibility for managing issues and making complex trade-offs with both internal and external stakeholders.
* Acting as a sponsor to support and manage the implementation of supply chain change and being the first point of contract for Senior Stakeholders within the organizations regarding your portfolio of products
Essential for the role
* Education acc. to CV.
* In depth knowledge of supply chain and the drug development process.
* In depth knowledge of Clinical Development processes relevant to investigational products.
* Awareness of GXP Standards within a clinical environment
* Proven experience of demand management and forecasting
* In depth experience of project management and influencing and managing 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 for the role
Working knowledge of the Clinical Trial Directive and global regulatory environment impacting the provision of investigational products. As well as, experience in lean methodology and tools.
Why AstraZeneca?
At AstraZeneca we're dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There's no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration, and always committed to lifelong learning, growth and development. We're on an exciting journey to pioneer the future of healthcare.
What's next!
Are you ready to bring new ideas and fresh thinking to the table and be part of our excellent team! We welcome your application (including CV and cover letter) no later than April 11th, 2023.
Ersättning Not Specified
Så ansöker du Sista dag att ansöka är 2023-04-07
Klicka på denna länk för att göra din ansökan Arbetsgivarens referens Arbetsgivarens referens för detta jobb är "R-162620".
Omfattning Detta är ett heltidsjobb.
Arbetsgivare Astrazeneca AB (org.nr 556011-7482)
Arbetsplats AstraZeneca
Kontakt AstraZeneca
galia.nystrom@astrazeneca.com Jobbnummer 7596187
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