At a Glance
- Tasks: Audit clinical sites and ensure compliance with GCP and CSV standards.
- Company: Leading UK biotech company focused on innovation and quality.
- Benefits: Hybrid work model, competitive salary, and opportunities for professional growth.
- Other info: Collaborative environment with a focus on continuous improvement.
- Why this job: Join a dynamic team and make a difference in the biotech industry.
- Qualifications: Experience in QA auditing and knowledge of GxP regulations.
The predicted salary is between 50000 - 65000 £ per year.
Talentmark is partnering with a UK biotechnology company to recruit a QA Auditor or Senior QA Auditor with a focus on GCP/clinical site auditing and CSV auditing.
The role offers hybrid work with 3 days on-site and a competitive salary.
You will maintain and enhance the Quality Management System, ensure Gx P compliance, and support regulatory training, e QMS and QA projects within the organisation.
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Senior QA Auditor – GCP/CSV, Hybrid, Biotech in 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.
