Quality Validation and CSV Manager

Quality Validation and CSV Manager focuses on we have invested heavily in industry 4.0 state of the art bespoke equipment to support sustained new product introductions and volume increases.

What the role involves

• We have invested heavily in industry 4.0 state of the art bespoke equipment to support sustained new product introductions and volume increases.
• Managing the planning, execution, and maintenance of validation activities (including process, cleaning, facility, and Computer Systems Validation, and equipment qualification).
• Ensure validation activities comply with regulatory expectations, GSK quality standards (QMS), and industry best practices (maintaining audit readiness at all times).
• Provide technical expertise for validation and CSV processes.
• Collaborate with cross-functional teams (including Engineering, Manufacturing, IT, and Quality teams) to ensure validation activities align with project timelines and business obje.
• Review, and approve validation protocols, reports, and associated documentation, ensuring accuracy, compliance, and adherence to validation requirements.

Skills and requirements

• Degree in relevant Scientific, Technical or Engineering discipline (or equivalent experience, ideally gained working in a manufacturing facility within a highly-regulated industry).
• Relevant knowledge/experience within Validation and CSV.

Confirmed role details

• Competitive base Salary.
• Annual bonus based on company performance.
• Opportunities for support for professional development and chartership.
• Access to healthcare and wellbeing programmes.

Additional role context

• As a key supplier of some of GSK’s blockbuster products the site contributes revenues of ~$2Bn annually.
• Direct Reports – The role manages approximately 9 to 12 direct reports.