Hays is now looking for a consultant to take on the role of Clinical Supply Associate at AstraZeneca in Mölndal for 12 months. 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. 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 Associate (CSA) 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 who thrives working in a task based, agile and global environment. What you'll do The CSA supports GCSC teams with task-based activities that include: * Timely management of temperature excursion assessment affecting clinical trial material. * Coordination of the country release requests of study labelled material. * Electronic document archiving and quality control. * User Acceptance Testing of digital systems. * Support the coordination of the purchase and delivery of External Commercial Products. * Facilitation of documentation activities ensuring inspection readiness to meet international GMP standards. * Documentation and coordination of product complaints and GMP deviations. * Utilising Supply Chain Management systems to support agile ways of working. * Continually improving the Clinical Supply Chain processes through visual management, problem solving, global standardisation and process confirmation. In this role you will have the opportunity to develop leadership skills and enterprise acumen, quickly becoming a Super User within a core role and/or leading improvement initiatives. You will 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. So, what's next! Are you already imagining yourself joining our team? Good, because we can't wait to hear from you. Skicka ansökan