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  • Job type

    Temporary
  • Location

    Macclesfield
  • Working Pattern

    Full-time
  • Specialism

    Drug Safety And Pharmacovigilance
  • Industry

    Pharmaceuticals
  • Pay

    £370 per day (UMB)

Pharmaceuticals | Analytical Chemistry | Full-Time | On-Site

Your new company

A global, science-driven biopharmaceutical company dedicated to discovering, developing, and delivering innovative, meaningful medicines and healthcare solutions that enrich the lives of patients.


Your new role

  • You will be the first point of contact for the analytical aspects of development and supply of drug products for use is early clinical studies.
  • You will work with other skill areas such as formulation and solid state to ensure the appropriate characterisation is performed to influence the development of drug products.
  • You will ensure high quality methodology is in place to characterise drug products and generate the high quality analytical data we need to progress projects.
  • You will have the opportunity to work with scientists in other functions to drive science and innovation within drug projects; this will include collaboration with scientists at our Cambridge, Boston & Gothenburg sites.

What you'll need to succeed

  • Lead the analytical development activities to support development and supply of drug product during the early clinical phases.
  • Identify and develop the analytical methodologies that support project progression through early development.
  • Conduct lab-based experimental work to generate data to support progression of your own and other projects.
  • This will include compliance with Good Manufacturing Practice where appropriate.
  • Interpret analytical data and draw reliable conclusions and recommendations to influence project progression.
  • Develop the risk assessments and stability and control strategies that ensure our patients receive a safe and efficacious drug product.
  • Author the relevant sections of regulatory submissions and prepare responses to regulatory questions.
  • Work as a member of cross-functional teams, representing EPDM or an area of your expertise.
  • Compliance with appropriate Safety, Health & Environment (SHE) and Quality (e.g. Good Manufacturing Practice , GMP)

You MUST have experience in the pharmaceutical industry.


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