Senior QandV Specialist

Senior Qualification and Validation (QandV) Specialist Our client is a global pharmaceutical manufacturer with a major GMP-regulated production site in Central Scotland. As part of continued investment in their Quality organisation, they are looking to appoint a Senior Qualification and Validation Specialist to strengthen governance and compliance across site QandV and Periodic Review activities.The RoleReporting into the site Quality function, you will take ownership of key QandV quality system elements, coordinating, maintaining and promoting QandV compliance across the site. You will lead and support continuous improvement of related quality and operational systems, ensuring the site and its functions remain compliant with GxP regulations and applicable quality guidelines, including UK/EU/US GMP/GDP, ICH, ISPE and other region-specific requirements.Key ResponsibilitiesProvide planning, support and guidance for validation projects, including continuous improvement of validation policies, procedures, templates and working practices.Oversee project plans and milestones alongside project teams to meet compliance and customer requirements.Coordinate resourcing and facilitate validation projects across the site.Provide validation expertise, advice and guidance to the site, the QandV team and third parties, ensuring compliance with site policy and procedures.Develop validation documentation with project teams in line with relevant SOPs and good practice, and facilitate review ..... full job details .....