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Process Engineer, MSAT

35 / per week - Full-Time
Cowley ,

Our Manufacturing Sciences and Technology (MSAT) team is delighted to be able to offer GMP manufacturing professionals the opportunity to challenge themselves within a cross functional role.

Oxford Biomedical is a pioneer of gene and cell therapy and our work is helping to deliver life changing treatments.

Gene and cell therapy is the treatment of disease by the delivery of therapeutic DNA into a patient’s cells, providing long term and potentially curative treatments for a wide range of diseases. With the potential to transform medicine, the sector holds significant promise with the first commercial products now launched and others rapidly approaching the market

Using your emerging knowledge and working alongside an established team of MSAT scientists you will be providing technical and scientific support to our clinical and commercial manufacturing and third carried out either in-house or by third party CMO’s on behalf of Oxford Biomedica

Key Duties & Responsibilities:

  • Support root cause investigations using a systematic approach to resolve complex problems and implementing solution.
  • Gather, evaluate and analyse process data for manufacturing process robustness.
  • Partnering with other functions to ensure scale-up is robust and scientifically sound leading to consistent performance
  • Support cross-functional activities working across Research, Process R&D, Manufacturing, Supply Chain and Quality Groups
  • Technical reviewer of manufacturing documentation (batch manufacturing records, deviation handling, CAPA, change controls, SOPs, etc.)
  • Generate and review documentation supporting technology transfer and NPI. Define success criteria for technical transfer and provide expert evaluation of the technical outcomes

Person Specification:

  • Minimum post-graduate degree in Biology/Biochemistry, Chemical/Biochemical Engineering or previous time served experience within a GMP manufacturing environment
  • Previous experience within industrial Biologics within a GMP environment
  • Process development experience is an advantage
  • Experience in aseptic processing and/or fill & finish would be an advantage
  • Demonstrable ability to consult and challenge cross functionally.

We look forward to hearing from you.

No agencies please.

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