Genetic Toxicology Lab Technician – In Vivo Studies

HAR Labcorp Early Development Laboratories Limited

Huntingdon

Presencial

GBP 25.000 - 35.000

Tempo integral

Há 3 dias
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Benefícios oferecidos por esta vaga

Competitive salaries
No weekend work
Wider benefits package including/p>

Resumo da vaga

Labcorp is seeking a Laboratory Technician to join the In Vivo Genetic Toxicology team at Alconbury, near Huntingdon, Cambridgeshire. The role involves GLP-compliant study work, data recording, QC checks and routine lab tasks within a Monday–Friday, 37.5-hour schedule.

You will support a range of in vivo and in vitro safety tests, develop lab skills, and contribute to the accuracy and efficiency of study processes in a regulated environment.

Qualificações

  • GCSEs of grades C/4 or above in Maths, English and Science.
  • Degree in Biology, Biomedical Science or Biochemistry preferred.
  • Teamwork and effective communication skills are important for this role.

Responsabilidades

  • Perform study work in accordance with Study Plans, SOPs and GLP.
  • Meet deadlines by planning and completing routine tasks.
  • Ensure data accuracy and perform QC checks after training.
  • Maintain safe working practices under HASAWA and COSHH and seek improvements.
  • Report any difficulties or findings to the Study Director or senior staff.
  • Learn a broad range of standard laboratory skills and techniques.
  • Maintain routine lab tasks like cell stocks, reagents and calibration checks.
  • Conduct stock takes and order lab products.
  • Prepare study files and documentation for GLP studies (e.g., In vivo micronucleus test).
  • Support both in vivo and in vitro safety assessment studies as needed.

Conhecimentos

Attention to detail
Teamwork
Communication

Formação

GCSEs in Maths, English and Science (C/4 or above)
Degree in Biology / Biomedical Science / Biochemistry

Descrição da vaga

Labcorp is seeking a Laboratory Technician to join the In Vivo Genetic Toxicology team at Alconbury, near Huntingdon, Cambridgeshire. The role involves GLP-compliant study work, data recording, QC checks and routine lab tasks within a Monday–Friday, 37.5-hour schedule.

You will support a range of in vivo and in vitro safety tests, develop lab skills, and contribute to the accuracy and efficiency of study processes in a regulated environment.

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