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