OGT is a leading global provider of clinical and diagnostic genomic solutions. We believe in creating products and partnerships that enable clinicians to deliver personlaised healthcare to patients and that empower clinical researchers to develop the next generation of precision medicines.

An opportunity has arisen for a Validation and Verification Analyst to join our Regulatory, Medical & Quality team on a 10-month fixed term contract. 

Our Regulatory, Medical & Quality team are responsible for ensuring that OGT’s products are safe, effective and fit for purpose, thus allowing them to be available globally and state of the art. 

Reporting to the V&V Team Leader, you will play an integral role in all laboratory aspects of the Validation & Verification Team and the delivery of internal technical and analytical performance data for a range of OGT products.

Your duties will include:

  • Responsibility for the smooth and efficient functioning of the laboratory, including consumables, reagents, microscopes, equipment and software
  • Laboratory duties include biological sample culturing, G-Banding and Fluorescent In Situ Hybridisation (FISH) slide-making and processing, image capture, receipt/logging of external samples, maintenance/use of internal samples and accurate up keep of laboratory records
  • Responsibility for an assigned proportion of the V&V FISH processing workload, using Formalin Fixed Paraffin Embedded (FFPE) sections, haematological and prenatal specimens
  • Contributing to the analytical workload within the V&V team, using in-house or external specimens as required (e.g. FFPE, haematological and prenatal specimens), using manual microscopes and automated software
  • Reporting of analytical results and upkeep of record and image databases
  • Contributing to the documentation and infrastructure by assisting with report writing
  • Responsibility for an appropriate proportion of the quality management system, including procedures and audits.

You will have:

  • A background in a Science related subject, preferably to A level or equivalent qualification. A degree level or equivalent qualification is desirable
  • Demonstrable experience of working in a GLP environment
  • Experience/knowledge in FISH processing and clinical FISH analysis of various sample types, including haematological and FFPE
  • An ability to use your scientific knowledge to problem solve and trouble shoot technical laboratory issues
  • Good attention to detail
  • An organised methodological approach to working, being able to manage your daily/weekly workload
  • Work well both individually and under supervision.
  • The ability to follow detailed processes

In return you will receive:

  • Competitive salary
  • Pension Scheme (10% non-contributory)
  • Private Health Insurance
  • Private Dental Insurance
  • Group Income Protection
  • Group Life Assurance
  • Pro-rata of 25 days holiday plus UK bank holidays
  • High Street Discount Scheme.

Application is via CV & a one-page covering letter outlining your suitability for the role, salary expectations and notice period

Please note that we will need to establish your right to work during the recruitment process.

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