Validation Specialist

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Validation Specialist

GxPeople are partnered with a Pharma company to join on a 12 month contract.


The Validation Specialist has a key role in ensuring the ongoing validation compliance of equipment, systems and processes.



  • Generates validation documentation (protocols/reports) and provides assistance with the execution of protocols for equipment, process, cleaning, utility, methods, and computerised systems.
  • Participates in the change control process advising on validation issues, as appropriate
  • Hands on role in the development and execution of DQ, IQ, OQ and PQ activities.
  • Ensures projects are managed in compliance with all required legal requirements (Health & Safety, cGMP, construction, environmental etc).
  • Designs, implements and executes validation studies for manufacturing and control equipment. Additional responsibilities for critical systems and facilities as well as validation studies to satisfy regulatory compliance.
  • Ensure that the validation status of equipment and systems are in compliance with cGMP at all times.
  • Maintain validation documentation through the - Approval and implementation of changes to relevant systems and assist in generating validation/ revalidation plans - Generate/review/approve execution of the validation/revalidation plans
  • Review and approval of site change controls
  • Ensure compliance to cGMP at all times



  • Degree in Science (Chemistry, Micro. or Pharmacy preferred) or Engineering (Chemical/Mech/Elec)
  • 5+ years Validation experience in the pharma/medical device industry


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