Computer Systems Validation Specialist

Computer Systems Validation Specialist

• East Kilbride | Onsite 5 days a week | free parking
• Circa £50,000 + 10% Bonus + Additional Incentives

A Career-Defining Role in Healthcare Technology

This is a rare opportunity to join a fast-growing healthcare business that's reshaping how patients access essential treatments and services. With a strong operational footprint and a culture built around innovation, the organisation is investing heavily in its digital infrastructure-and this role sits right at the heart of that transformation.

As a Computer Systems Validation Specialist, you'll take ownership of validation and lifecycle management for a range of critical systems. You'll work closely with IT and Quality leadership to ensure systems are robust, compliant, and audit-ready-while helping shape internal practices to meet evolving regulatory expectations.

What You'll Be Doing

• Coordinating and carrying out validation for both custom-developed and commercial off-the-shelf systems used across regulated environments.
• Supporting system lifecycle management from planning through to retirement, ensuring documentation and compliance remain watertight.
• Conducting risk assessments to determine validation scope and strategy based on Good Practice relevance.
• Creating and maintaining validation documentation including user/functional requirements, validation plans, protocols, reports, and traceability matrices.
• Liaising with internal teams and vendors to deliver compliant system implementations aligned to Good Automated Manufacturing Practice (GAMP) and agreed standards.
• Acting as a key contact for audit and inspection activity, particularly around data integrity and system validation.
• Participating in disaster recovery testing for critical systems and assisting with contingency planning.
• Helping evolve internal policies, templates, and working practices to keep pace with regulatory expectations.

What You'll Bring

• A proven background in a similar role within IT, Engineering, Life Sciences, or a related domain.
• Familiarity with regulatory frameworks including GAMP and other relevant standards.
• Experience working with both custom and off-the-shelf platforms in regulated (GxP) environments-such as in manufacturing, quality control, or clinical settings.
• Strong written documentation and stakeholder engagement skills.
• Confidence working across departments and communicating with both technical and non-technical audiences.

Why This Role Stands Out

• Be part of a mission-driven healthcare organisation with a strong growth trajectory.
• Work in a collaborative, forward-thinking team with clear leadership and direction.
• Enjoy a culture that values innovation, accountability, and continuous improvement.
• Benefit from flexible working hours, free food and drinks onsite, a cycle-to-work scheme, and a vibrant social calendar.
• Real opportunities for career progression and professional development.

Interested in Learning More?

If you're ready to take the next step in your career and want to be part of a purpose-led organisation where your expertise truly matters, we'd love to hear from you.

Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.