Role Overview & Specifications

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



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

About Lgc Limited

Lgc Limited is an actively verified employer hiring talent across technology, engineering, and operations.

  • Headquarters: United States / United Kingdom
  • Company Size: 1,000+ employees
  • Trust Rating: 95 / 100 (Official Registry Audited)

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