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SRG is seeking a Senior Qualification & Validation Specialist to strengthen governance across site Q&V and Periodic Review activities in Central Scotland. You will lead validation systems, drive continuous improvement, and ensure compliance with GxP, ISPE and regional guidelines.
You will partner with QA, Q&V teams and external partners, delivering training, documents and actionable validation strategies to maintain site readiness and regulatory compliance.
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 & Validation Specialist to strengthen governance and compliance across site Q&V and Periodic Review activities.
Reporting into the site Quality function, you will take ownership of key Q&V quality system elements, coordinating, maintaining and promoting Q&V 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.