QC Analytical Chemist

The post holder will work as part of the Quality Control team to manage the analytical laboratory facility. They will take ownership for the efficient running of the Analytical Laboratory, ensuring it fulfils requirements of regulatory bodies, customers, and other departments. The role supports all equipment IOPQ activities and introduction of new laboratory equipment and software applications.

This role handles all aspects of the analytical laboratory, including product and raw materials testing and release, non-routine testing, documentation review, methods validation, housekeeping, reagents preparation, stock take, and ordering. There will be interaction with internal and external stakeholders to advise in analytical chemistry. Duties include supporting QC laboratory testing, release of final product and raw materials, and working closely with the onsite Validation Specialist.

The position involves full responsibility for operating and managing the lab in compliance with safety policy and cGMP, including equipment maintenance, calibration, and performance qualification. Analytical tests such as HPLC, GC, TGA, and UV will be performed routinely. Representation during customer and regulatory audits requires good knowledge of ISO, FDA, and MHRA requirements.

Opportunities include developing new methods, continuous improvement of existing methodology, methods validation, and writing procedures. Providing training to staff in analytical chemistry and QC areas supports team development. Involvement in customer complaints, problem solving, and RCAs offers chances to lead analytical projects.