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Computer Systems Validation Specialist
Job Posted: 2 days ago
Salary: £ 45,000 - 50,000 / Annum
Job Type: Permanent
Location: Glasgow
Expire in: a month
Job Description
Computer Systems Validation Specialist
East Kilbride | Onsite 5 days a week | free parking
Circa £50,000 + 10% Bonus + Additional IncentivesA 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.
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