Clinical Quality Associate Director - Cell Therapy

About this role

Responsibilities

• First-line quality oversight
• : provide direction and advice to Cell Therapy SMM teams on applying ICH-GCP, AZ standards and SOPs; support country leadership to plan and implement quality control activities.
• Quality metrics:
• develop, track and analyse quality metrics at regional/country level; identify trends and provide actionable insights to improve investigative performance and proactive issue management.
• Quality events and CAPA management:
• support investigations and, where applicable, approve quality events and CAPAs in Veeva Quality Vault.
• Training compliance and enablement:
• assess training compliance; deliver onboarding and ad hoc quality/compliance trainings, and foster an engaging quality culture.
• Inspection and audit support:
• consult at country level during RIST, inspections and audits; act as SME for CT SMM quality processes; contribute to inspection responses and readiness playbooks.
• Risk management:
• facilitate country quality risk registers; identify, calibrate and track compliance risks; escalate and define/support mitigation activities with SMM leadership.
• Collaboration for improvement:
• participate in CT Quality Network forums; work across the BPQL “triangle” (process-quality-learning) to embed quality considerations into process design and training materials.
• Essential for the role
• Bachelor’s degree (or equivalent experience) in a relevant discipline
• At least 4 years of relevant operational and/or quality experience in drug development within a pharmaceutical, biotech or clinical research environment
• Strong knowledge of ICH-GCP and major regulatory frameworks (FDA/EMA)
• Hands-on experience with quality events/CAPA management and related systems (e.g., Veeva Quality Vault)
• Ability to develop and use quality metrics and analytics to drive decisions and risk mitigation
• Experience preparing for audits/inspections and contributing to inspection responses
• Demonstrated stakeholder influence, collaboration across boundaries, problem solving, and communication skills
• Ability to manage multiple priorities, operate regionally, and maintain accountability and ownership
• Desirable for the role
• Good understanding and knowledge regarding Cell Therapy-relevant procedures eg experience with related therapeutic areas (haematology/multiple myeloma, transplant, or autoimmune disease such as MS, scleroderma, myositis, rheumatoid arthritis)
• Experience with process improvement methodologies (e.g., Lean Six Sigma) and/or business process design and management
• Broader understanding of Study Management disciplines and cross-functional clinical operations
• Experience supporting SMM or quality activities across multiple countries/regions
• Why AstraZeneca?
• At AstraZeneca we’re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There’s no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration, and always committed to lifelong learning, growth and development. We’re on an exciting journey to pioneer the future of healthcare.
• So, what’s next?
• Are you already imagining yourself joining our team? Good, because we can’t wait to hear from you.
• Are you ready to bring new ideas and fresh thinking to the table? Brilliant! We have one seat available and we hope it’s yours.
• Where can I find out more?
• Follow AstraZeneca on LinkedIn https://www.linkedin.com/company/1603/
• Visit our website:
• www.astrazeneca.com.au
• and our cell therapy careers page:
• https://careers.astrazeneca.com/cell-therapy
• AstraZeneca in Australia has been formally recognised as an Employer of Choice for Gender Equality by the Workplace Gender Equality Agency (WGEA) and as a Gold Tier Employer within the Australian Workplace Equality Index (AWEI). Visit our ANZ Careers Page -
• www.astrazeneca.com.au/careers.html
• to learn more about our commitment to fostering a flexible, diverse, and inclusive environment.
• We recognise that any recruitment process may present challenges, if there is anything we can do to make our recruitment process more accessible for you, please let us know via this
• Form
• .
• Date Posted
• 03-cze-2026
• Closing Date
• 02-cze-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.

About AstraZeneca BE

AstraZeneca is a global, science-led biopharmaceutical company that focuses on the discovery, development and commercialisation of prescription medicines, primarily for the treatment of diseases in four therapy areas – Oncology; Cardiovascular, Renal and Metabolism (CVRM); Respiratory & Immunology (R&I); and Rare Disease. Within Oncology R&D, AstraZeneca is investing in our internal capabilities to help us realise our ambition to become leaders in the delivery of next-generation cellular therapies. Leveraging historical expertise in biologics engineering, gene editing and immunology across solid and haematological malignancies, we are uniquely positioned to develop cutting-edge technologies to advance cell therapies in cancer treatment. What you’ll do As an Associate Director, Clinical Quality based in Sydney, you will join the Cell Therapy Clinical Operations (CTCO) Business Processes, Quality & Learning (BPQL) team, as part of the first-line quality pillar. Reporting to the Senior Director Cell Therapy BPQL, you will lead regional quality oversight activities for SMM, embedding GCP-aligned practices, driving training compliance and helping to develop quality metrics that surface risks early.  You will partner closely with SMM leadership, process owners and learning leads to provide expert quality advice and coaching, ensuring operational teams maintain high quality standards and are inspection-ready.