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Olujimi Shobande

Olujimi shobande

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location of Olujimi ShobandeRochester, England, United Kingdom
Phone number of Olujimi Shobande+91 xxxx xxxxx
Followers of Olujimi Shobande204 followers

  • Timeline

    Jan 1989 - Jan 1993

    Assay Development Scientist, Research and Development

    Serono Diagnostics UK (now Merck Serono)
    Jan 1993 - Jan 1995

    Consultant Biochemist, Research and Development

    Strato Consulting
    Jan 1995 - Jan 1996

    Policy Support Officer

    Department of Health
    Feb 1995 - Oct 1995

    Purification Scientist, Downstream Processing

    Lonza Biologics (formerly Celltech Biologics)
    Jan 1996 - Jan 2000

    Scientific Assessor,Post-Licensing Division, Product Information Unit

    Medicines and Healthcare Product Regulatory Agency (MHRA)
    Jan 2000 - Jan 2004

    Section Manager,Licensing Division, Data Classification and Validation

    Medicines and Healthcare products Regulatory Agency (MHRA)
    Current Company
    Jan 2004 - now

    Head of Regulatory Affairs, Medicines, Healthcare products and Intellectual Property

    SUERTE PHARMA LIMITED

  • About me

    Head of Regulatory Affairs, NSL Group

  • Education

    • University of wolverhampton

      1985 - 1988
      Bachelor of science (bsc) biological and biomedical sciences

      Dissertation: Benzyl Alcohol Oxidase from the terrestrial slug, Arion ater, Initial purification and characterisation

    • Ucl

      1988 - 1989
      Master of science (msc) biochemistry and molecular biology

      Dissertation: Effects of whole-heart ischaemia and post-ischaemic reperfusion on the levels of the major purine nucleotides in the steady-state Langendorf perfused rat heart.

  • Experience

    • Serono diagnostics uk (now merck serono)

      Jan 1989 - Jan 1993
      Assay development scientist, research and development

    • Strato consulting

      Jan 1993 - Jan 1995
      Consultant biochemist, research and development

    • Department of health

      Jan 1995 - Jan 1996
      Policy support officer

    • Lonza biologics (formerly celltech biologics)

      Feb 1995 - Oct 1995
      Purification scientist, downstream processing

    • Medicines and healthcare product regulatory agency (mhra)

      Jan 1996 - Jan 2000

      • Scientific Assessor,Post-Licensing Division, Product Information Unit

        Jan 1998 - Jan 2000

      • Scientific Classifier, Post-Licensing Division, Variations and Renewals Tracking Unit (VRT)

        Jan 1996 - Jan 1998

    • Medicines and healthcare products regulatory agency (mhra)

      Jan 2000 - Jan 2004

      • Section Manager,Licensing Division, Data Classification and Validation

        Jan 2002 - Jan 2004

      • Team Leader, Licensing Division, PLUS Data Review

        Jan 2000 - Jan 2002

    • Suerte pharma limited

      Jan 2004 - now
      Head of regulatory affairs, medicines, healthcare products and intellectual property

  • Licenses & Certifications