Specialist Quality Assurance - 12 Month Secondment/FTC

Specialist Quality Assurance – 12 Month Secondment/FTCSpekePioneer a ‘new’ Quality wayAs the voice of the patient, every batch we certify is a personal stamp of approval. Not something we take lightly, we are always innovating, trialling the latest models and technologies to improve reliability and excellence in our processes.As QA Specialist you will act as a subject matter expert within QA providing technical and analytical support to the Quality Assurance function within the Speke site in addition to the wider site and global AZ partners. You will be responsible for the management and execution of quality documentation, compliance and quality system business processed within the quality technical department.We'll look to you to bring a focus on innovation, digital uplift, new technologies and sustainability practices across the documentation lifecycle as well as an expert knowledge and understanding of Good Manufacturing Practice.What you'll do:You will lead by example as a quality professional, supporting continuous improvement and compliance across key documentation and business processes. Your responsibilities include driving LEAN and digital initiatives, utilising process improvement tools, ensuring alignment with AZ standards, and proactively managing quality risks. You will coach others, share best practices, and help uplift capabilities across teams. You’ll also partner with cross-functional teams to meet documentation and compliance requirements, deliver efficient guidance, and actively contribute to regulatory and self-inspections.Essential Skills & Experience:Qualified to degree level / or equivalent in a scientific disciplineExperience in a Biopharmaceutical/pharmaceutical industryExperience in a cGMP environment (Quality assurance, Quality Control or Validation)Demonstrated knowledge on quality systemsExcellent technical writing and communication abilitiesTo be able to author standard GxP documentation independentlyAn understanding of the overall drug development and commercialization process from development, launch and through life cycle managementProject Management and Influencing skillsDemonstrated ability to work cross-functionally and to solve complex problemsAct as BPO for quality documentation and compliance and provide BPO oversite and management e.g. training, PMR and continuous improvementSo, what’s next…Are you already imagining yourself in this role? Good, because we can’t wait to hear from you!Date Posted26-Jun-2025Closing Date06-Jul-2025Our mission is to build an inclusive and equitable environment. We want people to feel they belong at AstraZeneca and Alexion, starting with our recruitment process. We welcome and consider applications from all qualified candidates, regardless of characteristics. We offer reasonable adjustments/accommodations to help all candidates to perform at their best. If you have a need for any adjustments/accommodations, please complete the section in the application form.

AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorisation and employment eligibility verification requirements.