Senior QA Auditor – GxP Compliance & Audits (Hybrid London)

Senior QA Auditor – GxP Compliance & Audits (Hybrid London)

London Full-Time 50000 - 65000 Β£ / year (est.) No working from home possible
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At a Glance

  • Tasks: Conduct internal audits and support regulatory inspections in a dynamic biotech environment.
  • Company: Leading UK biotechnology company focused on quality and compliance.
  • Benefits: Hybrid work model, competitive salary, and opportunities for professional growth.
  • Other info: Exciting opportunity for career advancement in a thriving industry.
  • Why this job: Join a collaborative team and make a real impact on GxP compliance.
  • Qualifications: Experience in QA auditing and knowledge of GCP and CSV activities.

The predicted salary is between 50000 - 65000 Β£ per year.

Talentmark is partnering with a leading UK biotechnology company to recruit a QA Auditor or Senior QA Auditor to join its Quality team in London.

The role focuses on maintaining the QMS, ensuring Gx P compliance, and supporting regulatory training, e QMS, and QA projects.

You will conduct internal audits across GCP and CSV activities, support regulatory inspections, and drive continuous improvement within a collaborative, hybrid environment.

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Senior QA Auditor – GxP Compliance & Audits (Hybrid London) employer: Talentmark

At Talentmark, we pride ourselves on being an exceptional employer, offering a dynamic work environment that fosters innovation and collaboration. Our hybrid model allows for flexibility while working with a leading global pharmaceutical company, providing employees with unique opportunities for professional growth in the fields of NLP and AI. With a strong emphasis on employee development and a supportive culture, we empower our team to make meaningful contributions to the scientific community.

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Contact Details:

Talentmark Recruitment Team

We think you need these skills to ace Senior QA Auditor – GxP Compliance & Audits (Hybrid London)

Quality Management System (QMS)
GxP Compliance
Regulatory Training
Internal Audits
Good Clinical Practice (GCP)
Computer System Validation (CSV)
Regulatory Inspections