Clinical Supply Coordinator to AstraZeneca
Poolia Sverige AB / Administratörsjobb / Göteborg
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hela Sverige 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. We are looking fpr a Clinical Supply Coordinator for a consulting assignment through Poolia Väst. The assigment will start in January 2023 and will dure one year. There might be possibilities to be extended.
About the position
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 Clinical Supply Chain Management.
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 recognizing their potential. Join us on our journey of building a new kind of organization 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.
Responsibilities
The CSC supports GCSC teams with task-based activities that include:
• Timely management of temperature excursions affecting clinical trial material.
• Facilitation of documentation activities ensuring inspection readiness to meet international GMP standards.
• Documentation and coordination of product complaints and GMP deviations.
• User Acceptance Testing of digital systems.
• Coordination of the ordering process for the manufacture of study labelled material.
• Utilizing Supply Chain Management systems to support agile ways of working.
• Continually improving the Clinical Supply Chain processes through visual management, problem solving, global standardization and process confirmation.
In this role you will have the opportunity to work with multiple customers and partners internally and externally across all phases of the drug development lifecycle, covering small and large molecule drug products. You will follow SHE and GMP standards, and will be personally accountable for these areas within your own work plans.
Your profile
We believe that you have the following background:
• A scientific / business / supply chain degree (or equivalent)
• Thrives in a process orientated workplace, on task based activities and with a focus on the customer.
• Organized 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 standardized processes and Lean improvement.
• Knowledge of Good Manufacturing Process and the drug development process.
About the organisation
The consulting role is suitable for you who want to gain broad experience. We offer you the chance to work in popular workplaces with well-known brands where you can develop your skills and broaden your CV. You will thrive as a consultant if you are looking for a world of exciting assignments and develop your network of contacts. By your side, you have your consulting manager who supports you in succeeding on your assignment. We want you to thrive and enjoy yourself with us at Poolia. Therefore, we offer you wellness grants, discounts on various fitness facilities and regularly social activities. Of course, your employment at Poolia includes collective agreements, insurance, occupational pensions and occupational health care.
Ersättning Fast lön
Så ansöker du Sista dag att ansöka är 2024-01-10
Klicka på denna länk för att göra din ansökan Arbetsgivarens referens Arbetsgivarens referens för detta jobb är "70351".
Omfattning Detta är ett heltidsjobb.
Arbetsgivare Poolia Sverige AB (org.nr 556426-7655),
http://www.poolia.se Arbetsplats Poolia Väst AB
Kontakt Emilia Malm
emilia.malm@poolia.se Jobbnummer 8366222
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