At a Glance
- Tasks: Lead global GCP audits and ensure compliance across clinical programmes and partners.
- Company: CPL Life Sciences, a leader in life sciences with a focus on quality and compliance.
- Benefits: Hybrid work model, competitive salary, and opportunities for international travel.
- Other info: Join a collaborative team dedicated to excellence in life sciences.
- Why this job: Make a significant impact on clinical quality and compliance in a dynamic environment.
- Qualifications: Strong experience with FDA, EU regulations, and ICH guidelines required.
The predicted salary is between 60000 - 80000 £ per year.
CPL Life Sciences is seeking an experienced Manager, GCP Auditing to lead risk-based auditing across global clinical programs, vendors and partners. You will partner with Clinical Operations, Quality, Regulatory Affairs and external partners to drive inspection readiness and ongoing compliance.
The role is Hybrid with international and domestic travel (30–40%), and requires strong experience with FDA, EU regulations and ICH guidelines to oversee audit strategies and CAPA activities.
We think you need these skills to ace Global GCP Audit Lead - Quality & Compliance Champion
GCP Auditing
Risk-Based Auditing
Inspection Readiness
Compliance Management
FDA Regulations
EU Regulations
ICH Guidelines
