SRG is recruiting a QA Officer for a well established GMP manufacturing site in Norfolk. You will join the QA team to help maintain high quality standards across processes and products.
Key duties include reviewing quality documentation, supporting CAPAs, investigations of GMP breaches, and assisting in QP batch release activities. The role offers exposure to continuous improvement projects in a regulated environment.
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GMP QA Specialist: Pharma & Med Devices 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.
