LGC Group
Biotech
ManufacturingAssociate
Neural analysis suggests this role is
optimal for mid candidates.
“Manufacturing Associate at LGC Group. Skills: Diagnostic product manufacturing, CGMP compliance. Apply direct labor. Manufacture diagnostic products”
Industry & Context.
Operator-level decisions
Lift up to 50 lbs, Weekend work, Off-hour work
What They're Looking For.
Must Have
High School Diploma, Basic mathematical skills, Ability to be on feet, Analytical and critical thinking skills
Nice to Have
1-3 years Life Science experience, CGMP/ISO environment experience, Clean rooms manufacturing experience, Bachelor's degree or equivalent, Biology or Chemistry concentration, Microsoft Office proficiency
What You'll Do.
Manufacture diagnostic products
Set up manufacturing equipment
Calibrate manufacturing equipment
Operate manufacturing equipment
Prepare products per procedures
Perform manufacturing processes
Adhere to safety policies
Maintain work area clean
Share improvement ideas
Support other departments
Lift and move materials
How You'll Work.
Team & Collaboration
Positive teamwork environment; Cross-training support
Full Job Description
ABOUT LGC CLINICAL DIAGNOSTICS: LGC Clinical Diagnostics develops and manufactures a comprehensive portfolio of catalogue and custom-developed diagnostic quality solutions and component materials for the extended life sciences industry. We partner with IVD assay developers, pharmaceutical, CRO and academic institutions in commercialization activities across the entire diagnostic pipeline. Laboratorians and diagnostic professionals across disciplines of clinical chemistry, immunochemistry, serology, molecular diagnostics, and clinical genomics 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. Each day, our world-class staff, scientific expertise, operational efficiency, and superior quality systems are ready to support the range of advanced technologies that collectively improve patient outcomes - from the widely adopted and established through to cutting-edge NGS and precision diagnostics. Job Purpose The Manufacturing Associate I applies direct labor for manufacturing high-quality diagnostic products using manual and semi-automated equipment. This role is responsible for setting up, calibrating, and operating all manufacturing equipment in line with cGMP, POPs, SOPs, Safety, and departmental policies. You will use good judgment and critical thinking skills to make operator-level decisions regarding product quality. Key Responsibilitie
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