At a Glance
- Tasks: Lead GCP compliance and manage audit programmes in a dynamic biotech environment.
- Company: Join a growing biotechnology company with an expanding clinical pipeline.
- Benefits: Competitive salary, flexible working hours, and opportunities for professional growth.
- Other info: Collaborative culture with a focus on career development and innovation.
- Why this job: Make a real impact on clinical quality assurance in a lean, innovative team.
- Qualifications: Experience in GMP and strong leadership skills in QA.
The predicted salary is between 75600 - 92400 £ per year.
Eblex Group is supporting a growing biotechnology company with an expanding clinical pipeline in the search for a Director Clinical Quality Assurance with GMP exposure. This broad QA role sits within a lean biotech environment and works closely with Clinical Development and other functions across clinical quality, audits, CAPA, investigations, QMS and inspection readiness.
As Director, you will lead GCP compliance, manage audit programmes, drive CAPAs and investigations, and provide QA input.
Director of Clinical Quality Assurance – Biotech GCP/GMP in London employer: Eblex Group
Eblex Group offers an exceptional opportunity for the Associate Director, Clinical Operations role within a dynamic and innovative rare disease biotech. With a strong emphasis on collaboration and cross-functional teamwork, employees benefit from a supportive work culture that fosters professional growth and development. Located in a fast-paced environment, this position allows for meaningful contributions to clinical development programmes, making it an attractive choice for those seeking impactful and rewarding employment.
