Onsite Senior Quality Validation & CSV Lead

GSK

Eggleston

On-site

GBP 55,000 - 75,000

Full time

3 days ago

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Job summary

GSK Barnard Castle in the United Kingdom is seeking a quality-focused professional to lead QA, NPI, validation and CSV activities across projects and operations. You will plan, execute and document risk-based quality activities, providing practical problem-solving and ensuring timely delivery with compliant processes.

This role requires a degree in science/engineering and hands-on experience in regulated validation, GMP, and batch documentation.

Qualifications

Degree in a scientific, technical or engineering discipline.
Practical experience in validation or QA in a regulated environment.
Experience in computerised system validation for IT/automation systems.
Working knowledge of GMP and quality management systems.
Experience producing and reviewing validation and batch release documentation.
Clear communication and ability to work with cross‑functional teams.

Responsibilities

Plan, lead and execute validation activities for processes, facilities, equipment and simple computerised systems.
Provide quality oversight for new product introduction, technical transfers and batch documentation.
Prepare and maintain validation protocols, test scripts, final reports and supporting evidence.
Make timely, risk-based quality decisions and communicate rationale to stakeholders.
Support inspections and close agreed actions.
Drive improvements to validation processes, templates and tools to increase efficiency and compliance.