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Kerry Child

Laboratory Manager

  • Managing a team of highly skilled Project and Senior Project Scientists to ensure regulatory-compliant method development and validation projects are delivered to a high standard, on time and within budget
  • Providing analytical support for Module 3 (Pharm Dev) of Market Authorisations (MAA) including device characterization work to support the CHMP (Committee for Medicinal Products for Human Use) guidelines
  • Managing resources efficiently and effectively to achieve the company's objectives and promoting a culture of continuous improvement to drive operational efficiencies
  • Ensuring links between onsite, cross-site and at-home workers are maintained so knowledge is shared and easily accessible
Having started with the company in 2011 as a QC analyst, I have worked in different teams over the years, working towards my current role as Laboratory Manager. I have extensive experience of working with Nicotine ENDS and pharmaceutical products, devices and clients in a heavily regulated environment (GMP/ISO17025). I am a skilled and accomplished leader that thrives under pressure, ensuring efficient prioritization of tasks to meet client expectations and often surpass them. Leading the Scientific Development team providing regulatory compliant method development, validation and investigation projects across e-cigarettes, HTP, CBD and pharmaceutical products, Study Director and Principal Investigator services for clinical studies and bespoke projects as an extension to our client’s Research and Development teams.

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