Global Clinical QA Auditor: Data Integrity & CAPA Leader in Maidenhead

Global Clinical QA Auditor: Data Integrity & CAPA Leader in Maidenhead

Maidenhead Full-Time 60000 - 80000 Β£ / year (est.) No working from home possible
Dormont Manufacturing Co

At a Glance

  • Tasks: Conduct global audits and ensure data integrity in clinical trials.
  • Company: Join CSL, a leader in biopharmaceutical innovation.
  • Benefits: Competitive salary, travel opportunities, and professional growth.
  • Other info: Dynamic role with a focus on risk-based quality assurance.
  • Why this job: Make a real difference in clinical research and quality assurance.
  • Qualifications: BS in biological science and GCP experience required.

The predicted salary is between 60000 - 80000 Β£ per year.

CSL is seeking a CQA Auditor to join its Research & Development Quality audit program in Maidenhead.

You will execute the global audit plan, assess site and vendor compliance, and ensure data integrity across clinical trials.

The role requires BS in a biological science, GCP experience, and willingness to travel up to 50%.

You will report findings, recommend CAPA, and help advance SOPs for risk-based quality assurance.

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Dormont Manufacturing Co

Contact Details:

Dormont Manufacturing Co Recruitment Team

We think you need these skills to ace Global Clinical QA Auditor: Data Integrity & CAPA Leader in Maidenhead

GCP Experience
Data Integrity Assessment
Audit Execution
Compliance Assessment
CAPA Recommendation
SOP Development
Risk-Based Quality Assurance