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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Submit ApplicationJob Details
- Location dalry, scotland
- Job Type Full-time
- Category Management & Operations
- Posted Date June 14, 2026
- Application Deadline July 24, 2026