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  • Job type

    Permanent
  • Location

    Greater Liverpool
  • Working Pattern

    Full-time
  • Specialism

    Quality Assurance And Validation
  • Industry

    Scientific and R&D
  • Pay

    £35,000 - £40,000
  • Closing date

    3 Jun 2024

Regulatory | Quality | Full-Time | On-site | Cell Therapy

We are recruiting on behalf of a client who is looking to add a quality and regulatory affairs specialist to their growing team.


Regulatory Requirements

  • Preparing submissions (GMP, MHRA, HTA).
  • Engagement with regulatory bodies.
  • Submitting licence approvals and maintaining these.
  • Knowledge of UK, EMA, FDA regulations.


Qualifications

  • Science or related degree.
  • Extensive knowledge of regulations/guidelines.


Benefits

  • 35 days holiday.
  • House loan scheme.
  • Flexible working.
  • Enhanced maternity/paternity package.
  • And more...


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