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- Tasks: Support quality processes for sterile medical devices and drive root cause investigations.
- Company: Dynamic Medtech company focused on innovation and quality.
- Benefits: Competitive salary, career growth, and hands-on experience in a fast-paced environment.
- Other info: Join a collaborative team and thrive in a regulated environment.
- Why this job: Make a real impact in the Medtech industry while working with cutting-edge technology.
- Qualifications: Experience with Class IIb/III devices and strong knowledge of ISO standards.
The predicted salary is between 28000 - 38000 £ per year.
We’re looking for a hands-on Quality / Manufacturing Engineer with strong experience in Class IIb/III medical devices to join a growing and dynamic team. This role is ideal for someone who thrives in regulated environments and enjoys working cross-functionally across production, quality, and suppliers.
Key Responsibilities
- Support manufacturing and quality processes for sterile medical devices
- Drive root cause investigations for manufacturing-related issues
- Manage and support CAPA, non-conformances, and complaints
- Work closely with production teams and external suppliers
- Lead and support change control processes
- Contribute to process validation and risk management activities
- Review and update SOPs and work instructions
- Participate in internal and external audits (front & back office)
Essential Requirements
- Experience with Class IIb/III devices
- Strong knowledge of ISO 13485 and 21 CFR 820
- Background working for a legal manufacturer or subcontract manufacturer
- Understanding of QC & GD&T on drawings
- Process risk management & validation
- Experience liaising with suppliers and production teams
- Proven audit experience (internal + external)
Desirable
- Validation protocol authoring
- Experience setting up new production lines/processes
- Exposure to additive manufacturing
- Engineering background
- Lead auditor training
- Experience in a start-up environment
- Authorship of procedures
If you're looking to make an impact in a high-quality, fast-paced Medtech environment, apply or reach out directly to learn more.
Graduate Engineer / Quality Engineer in London employer: Discover International
Contact Detail:
Discover International Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Graduate Engineer / Quality Engineer in London
✨Tip Number 1
Network like a pro! Reach out to professionals in the Medtech industry, especially those who work with Class IIb/III devices. Use platforms like LinkedIn to connect and engage with them; you never know who might have a lead on your dream job!
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of ISO 13485 and 21 CFR 820. Be ready to discuss how your experience aligns with the responsibilities of supporting manufacturing and quality processes for sterile medical devices.
✨Tip Number 3
Showcase your problem-solving skills! Be prepared to share examples of how you've driven root cause investigations or managed CAPA in previous roles. This will demonstrate your hands-on experience and ability to thrive in regulated environments.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive about their job search!
We think you need these skills to ace Graduate Engineer / Quality Engineer in London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to highlight your experience with Class IIb/III medical devices. We want to see how your background aligns with the key responsibilities mentioned in the job description.
Showcase Relevant Experience: When writing your cover letter, focus on your hands-on experience in regulated environments. Share specific examples of how you've supported manufacturing and quality processes in the past.
Be Clear and Concise: Keep your application clear and to the point. We appreciate straightforward communication, so avoid jargon and make sure your skills and experiences shine through without fluff.
Apply Through Our Website: Don’t forget to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for this exciting opportunity in our dynamic team.
How to prepare for a job interview at Discover International
✨Know Your Stuff
Make sure you brush up on your knowledge of Class IIb/III medical devices and ISO 13485. Familiarise yourself with the key regulations and standards, as well as any recent developments in the industry. This will show that you're not just a candidate, but someone who is genuinely interested and informed.
✨Showcase Your Experience
Prepare specific examples from your past experiences that highlight your skills in quality processes, root cause investigations, and CAPA management. Use the STAR method (Situation, Task, Action, Result) to structure your answers, making it easy for the interviewer to see how you can contribute to their team.
✨Cross-Functional Collaboration
Since this role involves working closely with production teams and suppliers, be ready to discuss your experience in cross-functional environments. Share examples of how you've successfully collaborated with different departments to solve problems or improve processes.
✨Ask Smart Questions
Prepare thoughtful questions about the company's quality processes, their approach to audits, and how they handle non-conformances. This not only shows your interest in the role but also gives you insight into whether the company’s culture aligns with your values.