LGC Clinical Diagnostics develops and manufactures a range of diagnostic quality solutions and component materials for the life sciences industry. We partner with IVD assay developers, and pharmaceutical, CRO and academic institutions in commercialisation activities across the entire diagnostic pipeline. Laboratorians and diagnostic professionals rely on LGC’s products to support accurate and reliable diagnostic results.

Our operating entities include Maine Standards Company, SeraCare Life Sciences, and Technopath Clinical Diagnostics, which are in vitro diagnostics (IVD) manufacturers of quality measurement tools (calibrators, controls, linearity, EQA/PT, biological materials), the Native Antigen Company, which is a manufacturer and supplier of viral antigens and LGC Proficiency Testing a global leader in PT schemes. We operate FDA-registered and ISO 13485-accredited facilities in Maine (USA), Massachusetts (USA), Maryland (USA), Tipperary (Ireland), ISO 9001-accredited facility in Oxford, UK, and Traverse City, Michigan US.

Our exceptional team, scientific skills, operational efficiency, and high-quality systems are primed daily to assist various advanced technologies, benefiting patient outcomes.

Job Purpose

Are you ready to be part of an exceptionally ambitious team working on innovative research? As a Production Assistant at LGC, you will play a key role in ensuring the flawless execution of our production processes. Your work will support the creation of high-quality products that compete on a global scale.

Key Responsibilities:

• Labelling, filling, and packaging of Multichem products with precision and care.
• Receipt, pooling, and filling of plasma, ensuring strict adherence to quality standards.
• Responsible for the accurate storage of supplies and products, maintaining an organized inventory.
• Daily cleaning of production equipment to ensure a pristine and efficient work environment.
• Assist in the manufacture of serum components and chemistry bases for QC controls, contributing to our world-class quality assurance processes.
• Ensure that all work is completed in a manner aligned with the requirements of ISO 13485, GMP, and the Technopath Quality Management System.
• Perform other related duties as assigned, demonstrating flexibility and a proactive approach to supporting our production team.

• Leaving certificate or equivalent, demonstrating your dedication to education and personal growth.
• Computer literacy, essential for efficiently managing production processes and documentation.
• Experience of working in an ISO 9001, ISO 13485, IMB/FDA regulated environment is desirable, showcasing your ability to successfully implement strict quality standards.

LGC is a top life science tools company, offering important solutions in growing markets.

Our values

• PASSION
• CURIOSITY
• INTEGRITY
• BRILLIANCE
• RESPECT

Benefits

• 25 days holidays
• Life assurance & health allowance
• Discounts with local and national retailers
• Free 24/7 Employee Assistance Programme
• Recognition schemes and monetary awards
• 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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