Validation Technician

Randstad Sourceright
10 Jan 2018
09 Feb 2018
Contract Type
Full Time

Validation Technician


Currently recruiting for a Validation Technician on behalf of a global, award winning Pharmaceutical company based in Irvine, Scotland.

Key Accountabilities:

The purpose of this role is to carry out the qualification and validation of processes, equipment, systems and analytical methods (existing, new or proposed) in accordance with the annual validation schedule and key responsibilities as follows:

  • Preparation of validation protocols in accordance with the validation schedule, company standards and current regulatory requirements
  • Co-ordination and execution of approved validation protocols; liaising with other departments on site as necessary to schedule the required activities in a timely manner to meet the validation schedule
  • Analysis of data and generation of validation reports, ensuring regulatory requirements are met
  • Preparation of a bi-weekly status report to monitor progress
  • Co-ordination of submission of samples for external analysis and monitors return of test results
  • Investigation and resolution of relevant deviations and CAPA plans relating to validation exercises and validated systems
  • Participation in root cause analysis involving validated systems
  • Active participation in the relevant change control and risk evaluation systems as they pertain to validation
  • Active participation in process improvement initiatives as required
  • Active participation in H&S risk assessments as they pertain to validation
  • Support site projects and new equipment purchases as required

Who you are:

  • Minimum of 2 years’ experience in a GMP manufacturing, QA OR QC position
  • Industry experience within Pharmaceuticals, Food & Drink or Oil

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