Company Description
LGC 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 Description
As a Production Biochemist at LGC, you will play a pivotal role in the flawless manufacture of our Multichem Control products. This hands-on position is crucial to our mission of delivering outstanding products and maintaining our reputation for quality and reliability. You will work closely with various departments, including Technical Directors and Sales teams, to ensure we meet our ambitious production targets and uphold our high standards.
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Manufacture and compound Multichem Control products to defined specifications.
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Analyse product performance and stability; troubleshoot and resolve issues.
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Coordinate production schedules and inventory requirements.
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Support new product introduction and provide technical input.
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Conduct QC testing and maintain compliance with GMP and regulatory standards.
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Strictly adhere to ISO 9001, ISO 13485, and IMB/FDA requirements.
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Collaborate with cross-functional teams to successfully implement continuous improvement initiatives.
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Determine and resolve production challenges to ensure flawless operations.
Qualifications
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Degree in Biochemistry or a related field, or equivalent experience.
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Strong understanding of clinical biochemistry and serum matrix interactions.
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Experience in ISO 9001, ISO 13485, and IMB/FDA regulated environments.
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Proven track record to optimise production processes and manage multiple projects.
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Excellent communication, problem-solving, and interpersonal skills.
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Ability to work collaboratively in a team-oriented environment.
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Ambitious and driven to achieve world-class results.
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Outstanding attention to detail and dedication to quality.
Additional Information
At LGC Clinical Diagnostics, you’re not just another employee—you’re a valued team member contributing to a better future. We offer:
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A collaborative, supportive environment where your ideas matter.
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Opportunities to work on impactful projects in the healthcare sector.
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A chance to grow professionally while making a tangible difference in people’s lives.
Benefits
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25 days holidays
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Life assurance & health allowance
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Discounts with local and national retailers
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Free 24/7 Employee Assistance Programme
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Recognition schemes and monetary awards
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Great long-term career opportunities
At 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!
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