This role will join a small team of validation and QA professionals, meaning it will be varied and allow good exposure to various aspects of validation. Client Details Our client is a Pharmaceutical manufacturer, long established in the market. Future plans look positive, and the business is forecasting strong growth Description - Support and co-ordinate the site validation master plan - Develop and author Commissioning, Qualification and Validation documentation - Perform various validation projects as dictated by the SVMP. This can include Process Validation, Cleaning Validation, CSV, and Equipment Validation Profile - Good level of exposure to various Validation projects in a GMP environment - Experience with Equipment Validation and Verification - Ability to work well within a team and be flexible with supporting others Job Offer - Competitive basic salary benefits