We support computer system validation projects in:
Pharmaceutical & Biotech Manufacturing – Validating manufacturing execution systems (MES), quality control software, and process automation in GMP production facilities, ensuring full regulatory compliance at every step.
Medical Devices & Diagnostics – Overseeing software and equipment validation for medical device production lines and diagnostic laboratories, maintaining rigorous documentation for audits under FDA and ISO 13485 standards.
Clinical & Research IT – Qualifying laboratory informatics platforms, clinical trial management systems, and electronic data capture tools in regulated healthcare environments to maintain data integrity and patient safety.
With over 20 years of life sciences recruitment experience, we understand what it takes to thrive in a GxP-regulated environment. Our specialist consultants know the validation standards and technical skills top employers are looking for and we’ll help you showcase yours. Thanks to our global network and trusted relationships with leading pharmaceutical and biotech companies, we often have access to exclusive CSV opportunities across North America, Europe, and Asia. We prioritise your goals and make the hiring process smooth and efficient, so you can focus on doing meaningful work that keeps systems validated, audit-ready, and running on time.
