SRG in Edinburgh is seeking a Junior QA Document Control Associate for a 3-month temporary contract. You will support the Quality Assurance team by digitizing, organizing, and verifying GMP documentation to ensure accuracy and integrity of records.
You will scan controlled documents, perform page-by-page quality checks, organize and index files, and assist with archival and retrieval activities while following GDP, ALCOA+, and company procedures.
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Temp QA Document Control Associate — GMP/GDP 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.
