At a Glance
- Tasks: Maintain and improve quality management systems while ensuring compliance with medical device regulations.
- Company: Join a leading medical device company committed to quality and innovation.
- Benefits: Competitive salary, health benefits, and opportunities for professional growth.
- Other info: Collaborative environment with a focus on continuous improvement and career advancement.
- Why this job: Make a real difference in healthcare by ensuring the highest quality standards.
- Qualifications: Experience in quality engineering and knowledge of ISO 13485 required.
The predicted salary is between 39600 - 48400 £ per year.
SRG in the United Kingdom seeks a motivated Quality Engineer to maintain and improve the QMS and ensure compliance with ISO 13485 and medical device regulations.
You will work cross-functionally with internal teams, suppliers, and external stakeholders to drive continuous quality improvements.
The role focuses on document control, CAPA, change control, risk management, internal audits, and product release processes, ensuring robust quality data analysis and proactive regulatory compliance.
Medical Device Quality Engineer – QMS & Compliance 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.
