Srg, a life sciences organisation in Stirling, UK, seeks a Quality Assurance Associate to support the QA function and ensure documentation excellence across the business.
You will review quality and batch documentation, provide document control, maintain trackers, and support archiving, while contributing to GMP/ISO compliance and QA improvements. This role suits someone with a data review background in regulated industries.
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QA Documentation Specialist – GMP/ISO Records 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.
