Join AstraZeneca in Gothenburg as a Clinical Supply Associate. Are you a team player with a problem-solving mindset and a focus on quality? AstraZeneca in Gothenburg is seeking a Clinical Supply Associate to join the team, offering an excellent opportunity to work in a task-oriented, agile, and global environment.Don´t miss the chance - Apply now for an exciting opportunity! Purpose, Offer and Benefits This is a consulting assignment for 1 year starting in May. You will be employed by TNG during the assignment period. Please note that selection will be ongoing. 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.  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. Your Responsibilities 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. The Bigger Picture 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. 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.   Our Expectations • Excellent communication skills. • A scientific / business / supply chain ambition. • Organised and structured with an excellent aptitude for digital systems. • Thrives in a process orientated workplace, on task-based activities and with a focus on the customer/patient. • Team player with a problem-solving mindset and a focus on quality. • Comfortable in a high paced and agile environment. • Ability to reflect, see the bigger picture, whilst also having a focus on the detail. Interested? This is a staffing assignment which means that you are employed by TNG, but work for one of our customers. If you are interested in this position, apply right now! The selection process is ongoing and the position can be filled before the last apply-date. If you have any questions, please contact the recruiter.