Job Description
Our client is driven by the pursuit of excellence and the mission to push the boundaries of cancer therapy. They are dedicated to delivering life-changing treatments to patients worldwide. Employees enjoy a flexible, diverse, and collaborative work environment that encourages creativity, leadership, and teamwork. The organization offers a competitive salary, performance-based bonus, comprehensive medical benefits, life insurance, pension contributions, and participation in an employee share program. Flexible working options are supported.
Role Summary
Our client is seeking a Quality Assurance professional to support the delivery of autologous CAR T-cell products for commercial and clinical use across the UK, EU, and US. This role is part of the central GMP manufacturing site’s QA team and will collaborate closely with internal stakeholders to ensure high-quality support and compliant operations.
Primary Responsibilities
1. Maintain GMP compliance within a multi-product facility supporting cell and gene therapy manufacturing.
2. Collaborate with cross-functional teams to uphold cGMP standards.
3. Review and approve validation documentation; escalate quality concerns as needed.
4. Ensure compliance within Validation, including periodic review of VMP trackers.
5. Author, review, and approve GxP documentati...