Production Biochemist

Job title:

Production Biochemist

Company

LGC Group

Job description

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 Description

• Assist in coordinating schedules and inventory requirements for control production
• Implement systems to support the generation and analysis of product performance data to monitor ongoing performance and stability of control products
• Assist in troubleshooting product problems as they arise on the floor; collaborate with Technical Director to resolve, correct and improve the product lines
• Liaise with sales staff on production requirements for analyte composition and targeting in all control products; monitor inventory of finished goods
• Technical support on the introduction of new products
• QC testing
• Adherence to regulatory and GMP requirements
• Additional duties as required

Qualifications

• Degree in biochemistry or equivalent and demonstrate a good understanding of clinical biochemistry
• Functional knowledge of interactions between proteins, enzymes, hormones and peptides in human serum matrices with regards to commutability and stability
• Experience of production operations and quality assurance requirements in an ISO 9001, ISO 13485, IMB / FDA regulated environment
• Proven track record in optimising production processes
• Strong project management skills with the ability to prioritise multiple tasks and projects

Additional 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.

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!#lgcij

Expected salary

Location

Tipperary

Job date

Thu, 20 Feb 2025 01:16:51 GMT

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