R&D Scientist, Clinical Chemistry & IVD Development

Randox Laboratories; Antrim; On-site; GBP 32,000 - 48,000; Full time

Job summary

Randox Laboratories is seeking an R&D Scientist for the Clinical Chemistry team in Antrim. The role focuses on development and optimisation of biochemistry-based IVD assays, supporting verification, validation, and lifecycle management of products.

The successful candidate will work on data generation, analysis, and documentation within a quality-managed environment, contributing to regulatory filings and manufacturing transfer as needed.

Qualifications

• Be qualified to at least undergraduate level in Biochemistry, Chemistry or a Life Science subject.
• Previous experience in analysis and documentation of large datasets.
• Previous laboratory experience or training.
• Excellent verbal and written communication skills.
• Proficient in the use of Microsoft applications (Word, Excel, PowerPoint and Outlook)

Responsibilities

• Support the development and optimisation of biochemistry-based IVD assays for established and novel biomarkers.
• Perform generation and analysis of assay performance data.
• Complete quality documentation in accordance with Randox QMS.
• Meet targets on established R&D projects.
• Familiarise with current methods and technologies on a given project.
• Prepare detailed reports demonstrating rigorous analysis of results.
• Contribute to continual improvement and assessment of existing products.
• Transfer of product to manufacturing per company procedures.

Skills

Biochemistry

Chemistry

Life Science

Data analysis

Communication skills

MS Office

Education

Undergraduate degree in Biochemistry, Chemistry or Life Science

Tools

Microsoft Office

Job description

Randox Laboratories is seeking an R&D Scientist for the Clinical Chemistry team in Antrim. The role focuses on development and optimisation of biochemistry-based IVD assays, supporting verification, validation, and lifecycle management of products.

The successful candidate will work on data generation, analysis, and documentation within a quality-managed environment, contributing to regulatory filings and manufacturing transfer as needed.