Scientist - Cell Potency

Scientist - Cell Potency

Intertek Pharmaceutical Services

Lancashire, United Kingdom

We need you to have

  • BSc/MSc/PhD in Biology/Chemistry (or related scientific discipline) is essential.
  • In-depth knowledge of Bioanalytical with over 10 years’ experience using cell-based bioassays for the analysis of biopharmaceuticals
  • Comprehensive experience of working in a GxP regulatory laboratory with strong understanding of GMP principles.
  • Strong method development and validation experience (ICH Q2 R1)
  • You should also be able to demonstrate experience training, supervising and coordinating the work of more junior scientists.

ABOUT THE OPPORTUNITY

Working within a diverse environment will provide an opportunity to utilise your skillset and knowledge to act as an independent member of the team. You will be expected to act as a lead investigator working across a vast array of projects which will range in scale, scope and timeline. You will take on accountability for becoming a technical reviewer and support with method validation, method optimisation and method development with some guidance. It will be necessary to work as an established member of the business providing guidance and support to more junior members of the team and passing on your knowledge and experience.

  • Competent in all practical aspects of cell-based potency bioassays covering one or more endpoints including cell proliferation, cell death, receptor binding, cell activation, gene transfection/transduction, ADCC and CDC
  • Expertise in plate-based bioassays and ideally one or more additional techniques including flow cytometry, ELISA, real time quantitative PCR, ddPCR
  • Providing analytical services to customers in the pharmaceutical and biopharmaceutical sectors in a GLP, GCP and GMP regulated laboratory.
  • Method development and validation in accordance with industry guidance.
  • Ability to work unsupervised, planning and performing analytical work, generating and interpreting data and generating reports when required.
  • Experience working with biopharmaceuticals eg. mAbs, bispecific antibodies, peptides, viruses, cell and gene therapies
  • Ability to assimilate and develop new techniques within the laboratory and work in new areas if required.
  • Good understanding of theoretical basis of the techniques and their application to biopharmaceuticals.
  • Ensuring bioanalytical studies meet the required quality standards and that are fit for purpose according to clinical phase and regulatory expectations.
  • Ability to problem solve autonomously without relying on specific written procedures; draw on literature to formulate best plan of action involving staff from other teams as necessary
  • Providing specialist expertise in method development, analytical method validation and sample analysis.

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