Clinical Supply Coordinator

Clinical Supply Coordinator

Arbetsbeskrivning

At AstraZeneca, we believe in the potential of our people and you’ll develop beyond what you thought possible! We make the most of your skills and passion by actively supporting you to see what you can achieve no matter where you start with us.

In Pharmaceutical Technology and Development (PT&D) 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.

The Clinical Supply Coordinator (CSC) supports Global Clinical Supply Chain (GCSC) to ensure the delivery of clinical material and associated information to meet the agreed clinical demand. This role is a great opportunity for someone wishing to embark on a career within Supply Chain Management.

About the position
The CSC supports GCSC teams with task-based activities that include:

• Coordination of the ordering of the manufacture of drug substance, drug product and packaged supplies, ensuring timely supply of clinical trial material to patients.
• Management of documentation activities ensuring inspection readiness to meet international GMP standards.
• Timely management of complaints and deviations.
• Utilise Supply Chain Management systems to support agile ways of working.
• Continually improve the Clinical Supply Chain processes through visual management, problem solving, standardisation and process confirmation.


Responsibilities
This role covers parts of the clinical study lifespan, across all phases of the drug development lifecycle, covering small and large molecule drug products.

In this role you will have the opportunity to work with multiple customers and partners internally and externally. You will follow SHE and GMP standards, and will be personally accountable for these areas within your own work plans.

Your profile
• A scientific / business / supply chain degree (or equivalent) with excellent grades
• Thrives in a process orientated workplace, on task based activities and with a focus on the customer.
• Organised and structured with an excellent aptitude for digital systems.
• Team player with a problem solving mindset and a focus on quality.
• Comfortable in a high paced and agile environment

Desirable Requirements
• Demonstrated understanding of the importance of standardised processes and Lean improvement.
• Knowledge of Clinical Manufacturing & Supply and the drug development process.

About the organisation
This position is a consultant assignment at AstraZeneca via QRIOS Life Science & Engineering in Göteborg for one year. During this time you will be employed by QRIOS Life Science & Engineering.
QRIOS employs curious experts in IT, Life Science and Engineering. We want to continue to attract the best employees, to continue to support our partners with the important competences you require. We are a recruitment and consulting company that is strongly inspired by those who never stop looking for new solutions. As we say, QRIOS MINDS GO FURTHER

At AstraZeneca when we see an opportunity for change, we seize it and make it happen, because any opportunity no matter how small, can be the start of something big. Delivering life-changing medicines is about being entrepreneurial - finding those moments and recognising their potential. Join us on our journey of building a new kind of organisation to reset expectations of what a bio-pharmaceutical company can be. This means we are opening new ways to work, pioneering ground-breaking methods and bringing unexpected teams together. Interested? Come and join our journey.

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