SRG in Edinburgh seeks a Temporary QA Document Control Associate to digitize, organize, and verify GMP documentation. You will scan controlled documents, ensure electronic records are complete, legible, and accurate replicas of paper originals, and maintain data integrity under established procedures.
The role requires attention to detail, strong organization, and the ability to follow GDP, ALCOA+ and company SOPs while maintaining confidentiality.
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QA Document Control Specialist - GMP Digitization (Edinburgh) 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.
