Hays AB jobb

This is a consultancy role for AstraZeneca for 12 months. Supply Chain Manager for Clinical Trial medications Would you like to utilise your planning and supply chain knowledge to lead clinical supplies for your portfolio of global clinical studies? With constant new products and launches, there has never been a better time to join Global Clinical Supply Chain and shape our future with a significant contribution to life-changing medicines. We have an exciting opportunity for talented Supply Chain Managers to join our Clinical Study Supply Chain team in Gothenburg, Sweden. This is a key role within our Clinical Manufacturing and Supply teams, and we make sure clinical trial medications are available at the right quality, in the right quantity at the right time for every patient taking part in AstraZeneca's trials all over the world. Our goal is to never miss a patient. In Pharmaceutical Technology and Development (PT&D) we are the bridge which turns forward-thinking science into actual medicines that helps 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. What you'll do: In this role you will project manage the design, plan, and set-up of the study supply chain to ensure on-time delivery of clinical supplies. You will also lead a cross-functional team enabling continuous dialogue with both internal and external partners on study design requirements and associated changes which may impact the supply chain elements of the study. To be successful in this role you need to be a fast learner, self-driven and comfortable working in a high pace R&D environment. You need to be a collaborative team player, flexible and have strong communication, planning and problem-solving skills. Your main responsibilities will include: * Project manage the delivery of clinical supplies effectively and consistently, and input to the balance of costs and any risks to supply. * Ensure effective communication with project teams and key partners across a global network. * Support risk management of individual studies with proactive mitigation of risks that potentially impact the quality or delivery of supplies. * Take ownership for Inventory management including any rework and recalls, extensions of shelf life and expiry date management, or stock destruction. * Manage the Interactive Response Technology (IRT) system to execute demand and supply planning. * Work within GMP Quality Management Systems ensuring that you actively handle any deviations, complaints and change controls. What you need to do now If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now. If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion on your career.

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.

Quality Release Manager / AstraZeneca / Södertälje / 11 months Hays is now looking for a consultant to take on the role of Quality Release Manager at AstraZeneca in Södertälje for 11 months. At AstraZeneca, we strive to continuously meet the unmet needs of patients worldwide. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality. If you are swift to action, confident to lead, willing to collaborate, and curious about what science can do, then you're our kind of person. Join the team where everyone feels a personal connection to the people that we impact. From our science labs to manufacturing at scale, we are committed to delivering at the highest quality. It's inspiring and rewarding work, influencing every part of the product lifecycle to deliver life-changing medicines! Welcome to External Quality (EQ), a global Quality organization within AZ Operations where the community is vibrant, and we never stop developing. We are now looking for a Quality Release Manager in the release team to help us manage release from external suppliers. This is a place where you will feel included in the conversation, where every voice is heard and makes a difference. What you'll do As a Quality Release Manager you will be accountable for product release for products manufactured by AZ external contract manufacturers, quality system element governance, change control, SOP management, and quality risk management. Additionally under your responsibility will be the maintenance of quality data and records in relevant quality management support systems. Your role will also involve facilitating process and system improvements and supporting audits and inspection requests for sites as well as handle deviation investigations and quality issue management. You will collaborate with colleagues and customers across many countries and interact cross-functionally with supply chain, technical, regulatory and project teams in AZ. Essentials for the role. * Masters degree in a science / technical field such as Pharmacy, Biology, Chemistry or Engineering. * Minimum 2 yrs experience in either the pharmaceutical operations environment or pharmaceutical Quality Assurance role * Minimum 2 yrs demonstrated experience of release processes, the quality event process, change control process * Strong demonstrated knowledge of cGMPs, Quality Systems and the pharmaceutical supply chain environment. * Excellent oral and written communication skills [English and local language(s)] * Strong problem solving skills * Strong negotiating/influencing skills * Ability to work independently under their own initiative * Ability to be in the office in Gärtuna, minimum 3 days/week Desirable for the role * Experience working in a PCO/PET organization or Lean/Six Sigma training * Multi-site / multi-functional experience

Scientist In vivo Bioscience - AstraZeneca - Göteborg - 7 months We are now looking for a Scientist to join the In vivo Bioscience team within Research and Early Development, Respiratory & Immunology in Gothenburg, Sweden. Respiratory & Immunology is one of AstraZeneca's main therapy areas. From a research perspective we work to understand, treat, modify and ultimately cure respiratory and autoimmune diseases. In this role, you will focus on mouse models of inflammatory bowel disease (IBD). Key Duties and Responsibilities: As part of the team, you will plan, execute and analyse ex vivo samples generated from in vivo studies to progress our drug discovery projects and generate publishable scientific insights. You will actively take part in scientific discussions to add valuable inputs in experimental design and data interpretation. This is a mainly lab-based role where you will be involved in ongoing projects focusing on pre-clinical experiments. What you'll do: * As a Scientist you will be a vital member of the in vivo community and will contribute to the development and characterization of pre-clinical models of IBD to discover novel therapeutics. * You will contribute to the analysis of in vivo studies with a specific focus on FACS analysis. ntial discussion on your career.