Company DescriptionLGC Group is a leading provider of diagnostic solutions, partnering with IVD assay developers, pharmaceutical companies, CROs, and academic institutions worldwide. Our operating entities, including Maine Standards Company, SeraCare Life Sciences, and Technopath Clinical Diagnostics, operate FDA-registered and ISO 13485-accredited facilities across the globe.At LGC Clinical Diagnostics, we're dedicated to advancing science with our comprehensive portfolio of diagnostic quality solutions and component materials. We are committed to improving patient healthcare by offering products and services that support accurate and reliable diagnostic results.Our total quality control solution provides clinical laboratories with significant cost, handling and time savings, whilst delivering higher confidence in analytical testing methods. As a Production Biochemist in our ambitious team, you'll play a vital role in the manufacture of Multichem products to desired specifications, designing and calculating additions for control product compounding.Job DescriptionAssist in coordinating schedules and inventory requirements for control productionImplement systems to support the generation and analysis of product performance data to monitor ongoing performance and stability of control productsAssist in troubleshooting product problems as they arise on the floor; collaborate with Technical Director to resolve, correct and improve the product linesLiaise with sales staff on production requirements for analyte composition and targeting in all control products; monitor inventory of finished goodsTechnical support on the introduction of new productsQC testingAdherence to regulatory and GMP requirementsAdditional duties as requiredQualificationsDegree in biochemistry or equivalent and demonstrate a good understanding of clinical biochemistryFunctional knowledge of interactions between proteins, enzymes, hormones and peptides in human serum matrices with regards to commutability and stabilityExperience of production operations and quality assurance requirements in an ISO 9001, ISO 13485, IMB / FDA regulated environmentProven track record in optimising production processesStrong project management skills with the ability to prioritise multiple tasks and projectsAdditional InformationAt LGC Clinical Diagnostics, you’re not just another employee—you’re a valued team member contributing to a better future. We offer:A collaborative, supportive environment where your ideas matter.Opportunities to work on impactful projects in the healthcare sector.A chance to grow professionally while making a tangible difference in people’s lives.Benefits25 days holidaysLife assurance & health allowanceDiscounts with local and national retailersFree 24/7 Employee Assistance ProgrammeRecognition schemes and monetary awardsGreat long-term career opportunitiesAt LGC, we foster a culture of inclusion and collaboration. We believe that diverse perspectives lead to better outcomes and encourage applicants from all backgrounds to apply. We are an equal opportunity employer and offer reasonable accommodations to individuals with disabilities. If you require any adjustments throughout the recruitment process, please let us know.Join us in this unique opportunity to be part of a company that is leading advancements in the industry!#lgcij