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

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 technically and professionally, the chance to have your voice heard as they evolve and optimise their offerings, and a lot more.

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.
• Strong written documentation and stakeholder engagement skills.
• 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!