Job Description

Job title – Lead Expert Validation

Location – Dalry, UK

Job model – On Site

Your key responsibilities

  • Leadership role within the Quality Department responsible for the management and co-ordination of the site cGMP validation activities.
  • Support validation activity during design, installation & commissioning of new equipment, processes, packaging lines & facilities and utilities.
  • Ensure the validated status of site facilities, i.e., equipment, processes, CSV and utilities is complete and compliant with internal local and corporate procedures, relevant regulatory requirements and industry guidance.
  • Authoring, reviewing, executing and maintaining validation documentation including site Validation Master Plan and Site Validation Strategy.
  • Support Production departments in validation activities for processes and equipment.
  • Preparation and management of validation plans, protocols and reports.
  • Supp...

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