SRG - IT - Administration

Automation Project Engineer needed in Devon to lead Controls & Automation projects within a fast-paced manufacturing environment. You will manage the full project lifecycle from design to commissioning, ensuring safety, quality, and budget adherence. Requires proven PLC/SCADA/HMI expertise (Allen...

Join a rapidly expanding speciality chemicals manufacturer as a Laboratory Manager in Shrewsbury. You will lead a team of 4 Chemists, manage R&D, Technical & QC projects, and drive innovation in sustainable, bio-based products. Ideal candidates have a Chemistry degree and proven lab management ex...

Quality Director sought for a senior leadership role at a leading GMP manufacturer in Skipton, UK. You will oversee site-wide quality operations, regulatory compliance, and strategic quality system development. Requires a Chemistry degree, extensive pharmaceutical GMP experience, and proven audit...

Join Synergy as a Stability Analyst at Reckitt in Hull, supporting health product stability studies in a GMP/GLP environment. Use HPLC, GC, and analytical techniques to deliver high-quality data for R&D teams. Ideal for candidates with a science degree and hands-on lab experience. Benefit from co...

Shift Analytical Chemist position available on a permanent basis in North Cheshire. You will join a multinational chemicals manufacturer, conducting GC, HPLC, and wet chemistry analysis on diverse samples. A valid driving licence and recent industrial analytical experience are essential. This rol...

We are seeking a Clinical Trials Associate to join our team in Hitchin, UK. You will take ownership of the Trial Master File (TMF), ensuring full regulatory compliance and inspection readiness. Ideal candidates have 2+ years of clinical trials experience, strong TMF management skills, and a solid...

Seeking an experienced **Associate Principal QA Specialist** in **Slough, UK** to provide expert GMP oversight and drive quality excellence. You will act as a **GMP Subject Matter Expert (SME)**, managing deviations, CAPAs, and change controls via TrackWise. Ideal candidates bring 5-10 years of Q...

Lead the Microbiology function at a growing GMP-regulated site in Glasgow. This key leadership role requires proven experience in a regulated lab environment, managing teams, and driving quality standards. You will oversee laboratory operations, support audits, and collaborate with cross-function...

Seeking a Project Engineer in Chester, UK, to lead the introduction of new automated manufacturing equipment within a highly regulated GMP environment. You will manage full lifecycle projects from specification through IQ/OQ/PQ validation, collaborating with cross-functional teams and vendors. Id...

Seeking an experienced **Project Manager** in **Chester, UK** to lead complex automation and change initiatives within a highly regulated manufacturing environment. You will manage full project lifecycles, budgets, and cross-functional stakeholders, ensuring timely delivery against GMP and qualit...

Join a leading biopharma manufacturer as an MSAT Bioprocess Specialist in Falkirk. You will lead biologics technology transfer, scale-up, and GMP documentation within a robust Quality Management System. The role requires a Science/Engineering degree, proven GMP biologics experience, and strong pr...