At a Glance
- Tasks: Conduct audits and ensure compliance with GxP regulations in a dynamic biotech environment.
- Company: Join a leading UK biotechnology company making a real impact in the industry.
- Benefits: Enjoy hybrid working, competitive salary, and a comprehensive benefits package.
- Other info: Great opportunity for career growth in a supportive and collaborative culture.
- Why this job: Be part of a quality team driving continuous improvement and innovation.
- Qualifications: Degree in a scientific field and experience in Quality Assurance essential.
The predicted salary is between 49500 - 60500 £ per year.
- QA Auditor / Senior QA Auditor – CSV
- Hybrid | London | Permanent
Talentmark is partnering with an innovative UK biotechnology company to recruit a QA Auditor with CSV expertise to join its growing Quality team.
Our client is open to candidates at either QA Auditor or Senior QA Auditor level, depending on experience.
This is an excellent opportunity for an experienced Quality professional with Computer System Validation (CSV) auditing expertise and a GCP background in a clinical site auditing (esource, EQMS and LIMS systems).
The Role
You'll play a key role in maintaining and enhancing the organisation's Quality Management System, ensuring compliance with Gx P regulations and supporting continuous improvement across the business.
You will be also supporting with regulatory training, e QMS and QA projects.
Responsibilities
Planning and conducting internal audits across GCP and/or CSV activities.
Performing supplier and vendor audits where required.
Identifying compliance gaps and driving CAPA activities.
Supporting regulatory inspections and client audits.
Contributing to QA projects, quality systems and regulatory compliance initiatives.
Promoting quality culture and continuous improvement throughout the organisation.
Your
Background: Degree in a scientific or related discipline preferred.
Experience in Quality Assurance within the pharmaceutical, biotechnology or life sciences sector.
Internal auditing experience is essential.
Strong experience auditing GCP clinical sites and CSV (Computer System Validation).
Experience supporting regulatory inspections and external audits.
Good understanding of Gx P regulations and quality systems.
Why Apply?
Join a leading UK biotechnology organisation making a real impact.
Hybrid working (2/3 days on-site).
Competitive salary and benefits package.
Apply
It is essential that applicants hold entitlement to work in the UK. Please quote job reference (Apply online only) in all correspondence
QA Auditor - CSV 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.
