Compliance Lead GCP/GLP

Our client, a leading pharmaceutical organization, is seeking a Compliance Lead to drive GCP and GLP deviation and CAPA management. The role focuses on reinforcing a risk-driven quality culture across early development, clinical, and post-marketing research projects.

• Triage and register deviations within the quality management system while coordinating root cause analysis.
• Negotiate and coach robust CAPA plans with process owners and subject matter experts.
• Track progress toward timely closure and design comprehensive effectiveness checks.
• Produce KPI and compliance dashboards and perform trend analyses to detect recurrence.
• Influence internal and external stakeholders to embed inspection readiness practices.

What are we looking for?

• You have 5+ years of experience in the biopharmaceutical industry.
• You bring 3+ years of experience in clinical research, specifically within
  GCP
  ,
  GLP
  , or
  GVP
  domains.
• You possess hands-on experience managing non-compliance, including
  CAPA
  ,
  deviation management
  , and effectiveness checks.
• You have experience working with a
  QMS
  , such as
  Veeva
  .
• You bring strong expertise in
  root cause analysis
  and risk-based prioritization.
• You are fluent in
  English
  .

Nice to Haves

• Experience with
  KPI
  dashboards, trend analysis, and
  AI/ML
  concepts.
• Strong communication, organization, and presentation skills.