SRG is seeking a motivated Quality Engineer to maintain and improve the Quality Management System (QMS) for medical devices and ensure compliance with ISO 13485, MDR/EU guidance, and customer requirements. You will collaborate with internal teams and suppliers to drive continuous improvement, support product monitoring and release activities, and participate in audits and CAPA processes.
The ideal candidate will have hands-on quality experience in medical devices, strong data analysis skills,
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Quality Engineer - Medical Device QMS & Compliance in City of London 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.
