SRG is seeking a Senior Qualification & Validation (Q&V) Specialist for a global pharmaceutical manufacturer with a GMP-regulated site in Central Scotland. You will own key Q&V quality system elements, coordinate validation projects and maintain compliance with UK/EU/US GMP/GDP, ICH, ISPE and other requirements.
You will lead validation documentation, support protocol execution and Periodic Review activities, and develop training packages while staying current with regulatory expectations and
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Strategic Validation & Compliance Lead in Stirling employer: SRG
As a Senior Clinical Trial Manager at our company, you will thrive in a dynamic and collaborative work environment that prioritises innovation and employee development. We offer competitive benefits, a strong focus on professional growth, and the opportunity to work alongside industry leaders in a location renowned for its commitment to advancing clinical research. Join us to make a meaningful impact in the field of clinical trials while enjoying a supportive culture that values your contributions.
