SRG is seeking an experienced Quality Engineer to join a growing medical device business on an initial 6 month contract. You will help maintain and improve QMS in line with ISO 13485 and regulatory requirements, supporting product development and manufacturing worldwide.
Joining a cross‑functional team, you will drive CAPA investigations, root cause analysis, risk management, and continuous improvement across manufacturing and supply chain to ensure compliant, high‑quality medical technologies.
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Medical Device Quality Engineer - ISO & CAPA Expert (6mo) 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.
