Location : Barcelona - Spain (3 days working from the office and 2 days working from home) Introduction The Director, Cell Therapy Quality Manage ment ( Dir. CT QM ) role will work in a collaborative manner with other members of the Cell Therapy Clinical Operations (CTCO) Business Processes, Quality & Learning (BPQL) team in order to provide expert quality advice and coaching so as to support the successful delivery of Cell Therapy Programmes. The Dir. CT QM role will function to support the teams across CTCO in order to ensure that all CTCO trials are prepared for both internal and external audits and inspections. The Dir. CT QM role has a specific area of expertise within CTCO BPQL in the following manner: Work closely with CTCO Process Owners in order to ensure that any established processes adhere to AZ global quality standards. Deliver or drive the development of quality -related initiatives and continuous improvement programmes that would support improved Quality and C ompliance within CTCO trials and within CTCO-related processes and initiatives. F irst line of Q uality support to all CTCO trials and CTCO-related initiatives. To operate within established AstraZeneca Quality group, including but not limited to the Cell Therapy Quality Network (CTQN), and Process Quality, Learning & Transformation (PQLT). Accountabilities CT BPM work s closely wit h the BPQL team, ensuring: - Insights related to CTCO-specific p rocess-related issues requiring corrective actions are documented for potential future process improvements. - Process KPIs & measurement: Support de velop ment, using quality-related data to inform process and business improvement activities. - Perform effective ness checks as needed to support the remediation of study-related CAPAs and if needed to verify the uptake and adoption of new and changed CTCO-related processes. Escalate, as needed, to 2 nd Line Quality and the broader CTQN any issues or risks related t o any CTCO-related studies or initiatives Communicate on a routine basis, relevant quality-related insights and feedback to the greater CTCO organization Education, Qualifications, Skills and Experience Essential Bachelor of Science in an appropriate discipline or equivalent experience At least 7 years of relevant operational and/ or quality experience in Drug Development within a pharmaceutical or clinical background Strong knowledge of business process, technology and Clinical Study information knowledge Demonstrated time management acumen and proven skills to deliver responses and suppor Experience in working successfully and collaboratively with both internal and external partners Demonstrated strong written and verbal communication and influencing skills, negotiation, collaboration, problem solving, presentation, knowledge transfer (mentoring), conflict management and interpersonal skills Strong knowledge of Clinical Trials related international regulations, guidelines and standards (ICH GCP, FDA, EMA regulations and guidelines as minimum), as well as AZ internal standards and procedures, across functions Ability to effectively influence and communicate; ability to engage and collaborate across boundaries with problem solving focus Ability to manage multiple competing priorities, demonstrating a growth mindset, innovation, ownership and accountability Desirable Strong reputation within the business and industry Strong understanding and knowledge regarding Cell Therapy-relevant procedures Experience of utilizing standard process improvement methodologies (e.g. Lean Six Sigma) to identify root causes of process issues and identify areas of process improvement Experience in the development and management of Business Process to deliver business performance Date Posted 04-dic-2025 Closing Date 09-ene-2026 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 authorization and employment eligibility verification requirements.