GVP Quality Auditor - Pharmacovigilance Compliance in Maidenhead

GVP Quality Auditor - Pharmacovigilance Compliance in Maidenhead

Maidenhead Full-Time 50000 - 70000 Β£ / year (est.) No working from home possible
CSL

At a Glance

  • Tasks: Conduct audits to ensure safety data accuracy and compliance with regulations.
  • Company: Join CSL, a leader in biopharmaceutical innovation.
  • Benefits: Competitive salary, travel opportunities, and professional development.
  • Other info: Collaborative team culture with potential for career advancement.
  • Why this job: Make a difference in patient safety while working in a dynamic environment.
  • Qualifications: BS in biological science and experience in Quality Assurance.

The predicted salary is between 50000 - 70000 Β£ per year.

CSL is seeking a GVP Auditor to execute the global audit plan within their Research & Development Quality audit program.

This role ensures the accuracy of safety data and compliance with legal and corporate standards through audits of partners and internal functions.

The ideal candidate will have a BS degree in a relevant biological science and Quality Assurance experience in a GVP-regulated environment.

Strong communication skills and the ability to work collaboratively are essential.

This position may require up to 50% travel.

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CSL

Contact Details:

CSL Recruitment Team

We think you need these skills to ace GVP Quality Auditor - Pharmacovigilance Compliance in Maidenhead

GVP Auditing
Quality Assurance
Biological Science Knowledge
Safety Data Accuracy
Compliance with Legal Standards
Communication Skills
Collaborative Work