Clinical Quality Manager; m​/f​/d - Cell Therapy

Innovative, dynamic, and sustainable:
As one of the world’s leading research-based pharmaceutical companies, we at AstraZeneca offer the best opportunities for your personal and professional development. For us, it’s clear: when we see a chance for change, we seize it and make it happen. Because an opportunity, no matter how small, can be the start of something big. Delivering life-changing medicines is about being entrepreneurial—finding these moments and recognizing their potential.

With us, every single employee puts patients first.

Make an impact in advancing Cell Therapy by ensuring the highest standards of quality and compliance.

We are seeking a

Clinical Quality Manager (CQM) (m/f/d) - Cell Therapy

to join our Cell Therapy Clinical Operations (CTCO) team.

In this role, you will collaborate with the Business Processes, Quality & Learning (BPQL) team to provide expert guidance and coaching, enabling the successful delivery of Cell Therapy studies by the Site Management and Monitoring (SMM) organization.

The CQM (m/f/d) is responsible for developing, tracking, and analyzing quality metrics at a regional or country level. In this role, you will provide guidance and advice to Site Management and Monitoring (SMM) teams on applying GCP principles, ensuring their work meets the highest quality standards.

You will use regulatory guidance, global standards, and SOPs to offer compliance advice and identify opportunities for improvement. When needed, you will recommend and communicate these improvements to Business Process & System Owners (BPOs). Additionally, you will support SMM management by consulting on compliance learning needs and facilitating training delivery.

While overall accountability for quality remains with the SMM country leadership team, you will work in close collaboration with them and other functions to plan and implement quality control activities effectively.

As part of the Cell Therapy Clinical Operations (CTCO) Business Processes, Quality & Learning (BPQL) team, you will bring specific expertise in the following areas:

• Partnering with CTCO Process Owners to ensure all established SMM processes align with global quality standards.

• Leading or contributing to quality-related initiatives and continuous improvement programs that enhance compliance within CTCO trials and processes.

• Collaborating actively with the Director, Cell Therapy Quality Management to strengthen quality culture and compliance across the organization.

Typical Responsibilities

• Assess training compliance of local SMM teams as part of quality oversight activities; deliver onboarding and ad hoc training on quality and compliance topics.

• Share global process updates impacting local SMM team quality compliance in a timely manner.

• Facilitate resolution of compliance issues and promote best practices across CT SMM countries.

• Support investigations and approve reported quality events and CAPAs in Veeva Quality Vault (VQV), if applicable.

• Foster an engaging quality culture within CT SMM; develop and implement compliance improvement initiatives.

• Provide country-level consultation during RIST, inspections, and audits; act as audit coordinator for internal audits and serve as SME during sponsor and investigator site inspections.

• Act as a key member throughout the inspection process, including consultation for inspection responses.

• Analyze quality metrics and trends to improve performance and proactively manage issues.

• Participate in regional CT SMM leadership teams and facilitate quality review meetings.

• Identify, track, and escalate compliance risks; support risk mitigation activities and manage country quality risk registers.

• Escalate significant issues or risks to the Director, Cell Therapy Quality Management.

Your Profile

You bring a strong foundation in science and quality management, combined with hands-on experience in clinical operations. Ideally, you have:

• A Bachelor of Science in a relevant discipline or equivalent professional experience.

• At least 4 years of operational and/or quality experience in drug development within a pharmaceutical or clinical setting.

• Solid understanding of business processes, technology, and clinical study…