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The preparation and testing of samples for clinical and forensic PT/EQA schemes, ensuring that defined criteria and deadlines are met. Contribute to development projects.

Key responsibilities:

• Undertake the production of PT/EQA test samples and the associated quality control assessments.
• Control stock and purchase of laboratory consumables
• Monitor and prioritise work according to production and reporting deadlines
• Maintain laboratory records and documents according to current procedures
• Carry out development project work as allocated and actively coordinate development work accordingly.
• Contribute to achievement of current team and individual objectives
• Conform to laboratory and company health and safety procedures and prepare COSHH assessments.
• Actively identify areas for improvement, with respect to laboratory efficiency, productivity and quality.
• Carry out additional duties or tasks, as directed, that are commensurate with the role and position

Qualifications and Experience required:

• Degree or equivalent in a scientific discipline, preferable chemistry, biochemistry or related subject level, or an appropriate level of experience
• Proven track record of working within a laboratory environment
• Organisational ability
• Methodical and precise approach
• Flexible and adaptable
• Computer literate
• Ability to work on own initiative and as part of a team
• Previous experience of working with biological fluids advantageous