> Markdown version of [/jobs/ext/4161142-method-development-lead](https://www.wearedevelopers.com/jobs/ext/4161142-method-development-lead). Every page supports `.md` or `Accept: text/markdown`. Links point to the HTML versions so they work for humans too. Agent guide: [/agents.md](https://www.wearedevelopers.com/agents.md). --- # Method Development Lead - **Company:** Nexus - **Location:** UK - **Experience:** Expert - **Salary:** £60,000.0 - **Contract:** Permanent contract - **Skills:** Data Systems, Lynx, Minitab, GXP - **Published:** October 2, 2026 - **Apply:** https://www.collegerecruiter.com/job/2915884205-method-development-lead ## About the Role * Degree in Biochemistry, Biomedical Science, or related field., * 4+ years in a GxP laboratory (2+ years in management). * Expertise in HPLC, UPLC, LCMSMS, and chromatography data systems. * Proficiency in method development, optimisation, and validation. * Strong problem-solving and troubleshooting capabilities. * Knowledge of protein precipitation, SPE, and Liquid-Liquid extraction techniques. * Understanding of regulatory and GLP requirements. * Strong communication, organisational, and leadership skills. Preferred Skills * Experience with Design of Experiments (DOE) for method optimisation. * Proficiency in Minitab/statistical software. * Experience with Empower and Mass Lynx data systems. * GC experience and familiarity with regulatory inspections. ## Description We are seeking a highly skilled MS Method Development Lead to drive the development and validation of LCMSMS bioanalytical methods under GxP standards., * Key duties include: * Leading method development and validation as a subject matter expert. * Optimising analytical extraction techniques, chromatography methods, and LC columns. * Managing and mentoring the Method Development & Validation team. * Ensuring compliance with GLP, SOPs, and international guidelines. * Troubleshooting analytical methods and recommending improvements. * Overseeing cost-effective laboratory operations and consumable spend. * Writing and approving Methods of Analysis and transferring validated methods to analytical teams. * Supporting regulatory submissions and resolving regulatory queries. * Conducting investigations, implementing CAPAs, and driving continuous improvement. * Preparing, reviewing, and ensuring adherence to GLP SOPs. * Leading team meetings and staff development sessions.