Veranova is hiring a Temporary QA Document Control Associate in the United Kingdom. The role supports GMP documentation digitization, organization, and verification, ensuring accuracy and adherence to GDP and ALCOA+ principles. Requires attention to detail, ability to follow procedures, and data integrity.
12-week assignment with exposure to QA activities and document control tasks. The candidate will scan, verify, index, and upload documents into the EDM system, maintaining tracking logs and
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Temp QA Document Control Specialist – GMP Records employer: Veranova
At Veranova, we pride ourselves on fostering an inclusive and dynamic work culture that prioritises employee growth and well-being. Our commitment to quality and safety is matched by our industry-leading compensation packages, comprehensive health benefits, and opportunities for professional development, making us an exceptional employer in the pharmaceutical sector. Join us in our mission to innovate and improve patient lives while enjoying a supportive environment that values your contributions and encourages continuous learning.
