The role focuses on maintaining validated systems through structured validation processes (IQ/OQ/PQ) and serves as a bridge between technical software testing and regulatory compliance.
You must have several years of experience in Computer System Validation (CSV) or software validation in regulated industries (pharmaceutical, biotech, or medical devices).
You will have a strong understanding of FDA, EMA, and GMP regulations, 21 CFR Part 11, GAMP 5 guidelines & Data integrity principles.
You must also have experience of Laboratory systems such as LIMS and Chromatography Data Systems (e.g., Empower).
You will be familiar with validation lifecycle and documentation standards.
Please apply ASAP if this role is of interest
Salary description
£302.00 - £345.00 per day