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- Tasks: Support QMS integration and improve quality systems in a medical device company.
- Company: Join a growing medical device company that just completed an exciting acquisition.
- Benefits: Gain hands-on experience, mentorship, and exposure to global standards in a dynamic environment.
- Why this job: Perfect for engineering graduates eager to kickstart their career in MedTech and Quality Affairs.
- Qualifications: Degree in Engineering with project or internship experience in medical devices or quality.
- Other info: Work closely with experienced engineers and engage in real projects from day one.
The predicted salary is between 28800 - 48000 £ per year.
Graduate Opportunity – Quality Systems Engineer | Medical Devices
Are you an engineering graduate with a passion for medical technology? Have you worked on university projects involving medical devices, regulatory frameworks, or quality systems?
I’m recruiting for a brilliant entry-level Quality Systems Engineer role with a growing medical device company that’s just completed an exciting acquisition.
In this role, you’ll play a key part in helping integrate the newly acquired business’s Quality Management System (QMS) into the existing framework. Once that’s done, you’ll continue to support and improve the system, with lots of exposure to global standards like ISO 13485, MDR, and 21 CFR 820.
What you'll be doing:
- Supporting QMS integration projects alongside experienced engineers
- Helping standardise procedures and close compliance gaps
- Assisting with the transition to a digital QMS (eQMS) platform
- Managing key documents like SOPs and forms
- Getting involved with non-conformance reports (NCRs), internal audits, CAPAs, and supplier assessments
- Driving continuous improvements and process optimisation projects
- Learning how to prepare for external audits and regulatory inspections
What we're looking for:
- A degree in Engineering (Biomedical, Mechanical, or similar)
- University project or internship experience in medical devices, quality, or product development
- A keen eye for detail and strong organisational skills
- A willingness to learn about ISO standards, medical device regulations, and QMS best practices
- Great communication and teamwork skills
This is the perfect first step into MedTech for someone excited to build a career in Quality & Regulatory Affairs. You'll be mentored by a highly experienced team and get hands-on with real projects from day one.
Interested? Message me directly or apply with your CV – I’d love to tell you more!
Contact Detail:
GxPeople Global Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Engineer
✨Tip Number 1
Familiarise yourself with ISO 13485 and other relevant regulations. Understanding these standards will not only help you in interviews but also show your genuine interest in the role and the industry.
✨Tip Number 2
Network with professionals in the medical device field. Attend industry events or join online forums to connect with people who can provide insights and potentially refer you to opportunities at companies like ours.
✨Tip Number 3
Prepare to discuss any relevant projects or internships during your conversations. Highlight specific experiences where you contributed to quality systems or regulatory compliance, as this will demonstrate your practical knowledge.
✨Tip Number 4
Show enthusiasm for continuous learning. Express your eagerness to develop your skills in quality management systems and regulatory affairs, as this aligns perfectly with our company culture and the role's requirements.
We think you need these skills to ace Quality Engineer
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience, especially any university projects or internships related to medical devices and quality systems. Emphasise your engineering degree and any specific skills that align with the job description.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for medical technology and your eagerness to learn about Quality Management Systems. Mention specific experiences that demonstrate your attention to detail and organisational skills.
Highlight Relevant Skills: In your application, clearly outline your understanding of ISO standards, regulatory frameworks, and quality systems. Use examples from your academic projects to illustrate your knowledge and skills in these areas.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any errors. A polished application reflects your attention to detail, which is crucial for a role in quality engineering.
How to prepare for a job interview at GxPeople Global
✨Show Your Passion for Medical Technology
Make sure to express your enthusiasm for medical devices and technology during the interview. Share any relevant university projects or experiences that highlight your interest in this field, as it will demonstrate your commitment to the role.
✨Familiarise Yourself with ISO Standards
Since the role involves working with ISO 13485 and other regulatory frameworks, take some time to understand these standards. Being able to discuss them confidently will show that you are proactive and serious about your future in Quality Engineering.
✨Prepare Examples of Teamwork
The job requires great communication and teamwork skills, so be ready to share specific examples from your university projects or internships where you successfully collaborated with others. This will illustrate your ability to work well in a team environment.
✨Ask Insightful Questions
Prepare thoughtful questions about the company's QMS integration projects and their approach to continuous improvement. This not only shows your interest in the role but also your eagerness to contribute to the team's success.
