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 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!
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