CSV Specialist / Systems Validation Engineer - Glasgow - 50-60K plus bonus

Lorien; Glasgow; On-site; GBP 50,000 - 60,000; Full time

Benefits offered by this job

Great bonus scheme

Opportunities for professional progression

Job summary

A leading recruitment firm is seeking a CSV Specialist / Systems Validation Engineer in Glasgow. This role involves validating systems in regulated environments and supporting compliance and quality assurance processes. The ideal candidate has a background in IT or Life Sciences and experience with regulatory frameworks. The position offers a competitive salary of 50-60K plus bonus, with opportunities for professional growth and development.

Qualifications

• Experience in validation for custom and commercial systems in regulated environments.
• Knowledge of Good Automated Manufacturing Practice.
• Experience with both custom and off-the-shelf platforms in regulated settings.

Responsibilities

• Coordinate and execute validation for systems in regulated environments.
• Support lifecycle management ensuring compliance and documentation accuracy.
• Conduct risk assessments based on Good Practice relevance.
• Create and maintain validation documentation.
• Liaise with teams and vendors for compliant system implementations.
• Act as primary contact during audits and inspections.
• Participate in testing for critical systems.
• Evolve internal policies and practices per regulatory expectations.

Skills

Proven background in IT/Engineering/Life Sciences

Familiarity with regulatory frameworks

Track record in regulated environments

Confidence in cross-departmental communication

Job description

CSV Specialist / Systems Validation Engineer - Glasgow - 50-60K plus bonus

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This range is provided by Lorien. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

CSV Specialist / Systems Validation Engineer - Glasgow (onsite) - 50-60K plus bonus

• Requirement of 5 days per week onsite near Glasgow

Lorien’s client, a rapidly growing organisation with bases across the UK and overseas providing life‑saving products to people around the globe, is looking to secure the services of a CSV Specialist / Systems Validation Engineer to take ownership of validation activity across multiple regulated systems, working at the intersection of IT, Quality, and Operations. This is a site‑based role reporting into the Head of IT, with close collaboration with senior quality representatives and others.

In return, they’ll offer you not only a great bonus scheme, but ongoing opportunities to progress both technical and professionally (with plenty of great case studies of progression, promotion and more to hand already), the chance to have your voice heard as they evolve and optimise their offerings, and a lot more. If you’re liking what you’ve read so far, have a look at the finer details below:

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 lifecycle management from planning onwards, 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 such as user/functional requirements specs/validation planning/protocols/reports/etc.
• Liaising with internal teams and vendors to deliver compliant system implementations aligned to Good Automated Manufacturing Practice and agreed standards
• Acting as a key contact for audit and inspection activity concerning data integrity and system validation
• Taking part in DR 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

• Proven background in a similar role/s in IT/Engineering/Life Sciences/similar domains
• Familiarity with regulatory frameworks including Good Automated Manufacturing Practice and similar relevant offerings
• Track record of working with both custom and off‑the‑shelf platforms in regulated (GxP) environments — such as in manufacturing, QC or clinical settings
• Confidence working across departments and communicating with technical and non‑technical audiences

This is a great chance to join a fast‑moving, growth‑focused organisation that’s deeply committed to its mission, work in a collaborative environment with influence across multiple business units, and play a pivotal role in ensuring quality, compliance and continuity across core IT systems. Want to know more? Apply now with your latest CV and let’s set up a chat!

Seniority level

• Mid‑Senior level

Employment type

• Full‑time

Job function

• Information Technology
• IT System Testing and Evaluation

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