My client, a leading pharmaceutical manufacturing company, has an excellent opportunity for a Validation Specialist to join the team on a permanent basis. Reporting to the Quality Manager you will be responsible for - - Develop, implement, and execute validation projects ranging from stand-alone equipment to process expansion and new packaging facilities. - Ensure the validated status of site facilities, e.g. equipment and processes, are complete and compliant with internal local and corporate procedures, relevant regulatory requirements and industry guidance. - Authoring, reviewing, executing and maintaining validation documentation. - Supporting external audits including customer and regulatory inspections, presenting and explaining relevant validation information to inspectors/auditors. - Execute validation protocols and drive to completion any CAPA associated with non-conformances raised. - Use quality risk management tools to ensure that risks are appropriately identified, documented and managed. - Support validation activity during design, installation & commissioning of new equipment, processes, packaging lines & facilities and utilities. - Excellent technical documentation generation and review skills. The successful candidate will hold a Degree in a relevant science or engineering discipline and have extensive experience working in a similar validation role within a GMP regulated Life Science Industry. You must also have excellent communication and organisation skills and be confident with your ability to work independently and within cross functional teams. To apply please send your CV to BWSR (Brightwork Specialist Recruitment) offers the services of an employment agency for permanent roles and an employment business for temporary roles.