At a Glance
- Tasks: Lead GCP quality activities and ensure compliance in gene therapy projects.
- Company: CPL Life Sciences, a leader in innovative healthcare solutions.
- Benefits: Competitive salary, career advancement, and a dynamic work environment.
- Other info: Join a passionate team dedicated to transforming patient care.
- Why this job: Make a real difference in cutting-edge gene therapy while ensuring quality and compliance.
- Qualifications: Experience in GxP quality assurance and strong leadership skills.
The predicted salary is between 60000 - 80000 £ per year.
CPL Life Sciences is seeking an experienced Quality Assurance Lead (GxP) for a late-stage gene therapy programme based in London. This hands-on role covers GCP/GMP oversight, vendor management, inspection readiness, and a fit-for-purpose quality systems framework across clinical operations, external partners, and manufacturing.
You will lead GCP quality activities for a Phase III programme, oversee deviations, CAPAs, audits and inspections, and drive regulatory readiness.
GxP Quality Lead – Gene Therapy (Phase III, London) employer: Cpl Life Sciences
Cpl Life Sciences is an exceptional employer, offering a dynamic work culture that fosters innovation and collaboration within the vibrant streaming and entertainment sector. Employees benefit from immediate project impact opportunities, comprehensive training, and career growth in a cloud-oriented environment, making it an ideal place for those looking to advance their skills in data engineering while working with cutting-edge technologies.
