**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.
• Support ...