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For Companies At a Glance
- Tasks: Review and assess compliance of medical devices with EU regulations and standards.
- Company: Global leader in medical device regulation with a focus on innovation.
- Benefits: High salary, remote work flexibility, and international collaboration.
- Why this job: Make a difference in healthcare by ensuring the safety of medical devices.
- Qualifications: Degree in biomedical engineering or related field; experience in regulatory compliance.
- Other info: Join a dynamic team with opportunities for growth and global impact.
The predicted salary is between 43200 - 72000 £ per year.
We are seeking an experienced Technical Expert to join our global team, working with active medical devices under MDR 2017/745 and ISO 13485 standards. Electronics device and audit experience is recognised. This is a fully remote role, offering the flexibility to work from anywhere, while engaging with international clients and supporting the certification of a diverse portfolio of medical device manufacturers.
What You’ll Be Doing
- Reviewing technical documentation for active medical devices and assessing compliance with EU MDR 2017/745
- Evaluating Quality Management Systems (QMS) in line with ISO 13485
- Managing certification activities for an international portfolio of medical device manufacturers
- Collaborating with teams and clients across multiple regions to ensure consistent, high-quality compliance
What We’re Looking For
- Bachelor’s or postgraduate degree in biomedical engineering, biotechnology, biology, chemistry, pharmacy, bioengineering, or equivalent
Medical Device Electronics Regulatory Engineer in England employer: X4 Technology
Contact Detail:
X4 Technology Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Medical Device Electronics Regulatory Engineer in England
✨Tip Number 1
Network like a pro! Reach out to professionals in the medical device field on LinkedIn or at industry events. We can’t stress enough how valuable personal connections can be in landing that dream job.
✨Tip Number 2
Prepare for those interviews! Research common questions for regulatory roles and practice your answers. We recommend using the STAR method to showcase your experience effectively.
✨Tip Number 3
Showcase your expertise! Create a portfolio of your past projects and experiences related to medical devices and compliance. This will help you stand out and demonstrate your skills to potential employers.
✨Tip Number 4
Apply through our website! We’ve got a range of opportunities waiting for you, and applying directly can sometimes give you an edge. Let’s get you that job!
We think you need these skills to ace Medical Device Electronics Regulatory Engineer in England
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience with medical devices and compliance standards like MDR 2017/745 and ISO 13485. We want to see how your background aligns with the role, so don’t be shy about showcasing relevant projects!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about working in the medical device field and how your skills can help us achieve our goals. Keep it concise but impactful!
Showcase Your Technical Expertise: In your application, make sure to mention any specific technical skills or experiences that relate to electronics and regulatory processes. We love seeing candidates who can demonstrate their knowledge and expertise in these areas.
Apply Through Our Website: We encourage you to apply directly through our website for a smoother process. It helps us keep track of applications and ensures you get the best chance to join our amazing team!
How to prepare for a job interview at X4 Technology
✨Know Your Regulations
Make sure you brush up on the EU MDR 2017/745 and ISO 13485 standards. Being able to discuss these regulations confidently will show that you understand the compliance landscape for medical devices, which is crucial for the role.
✨Showcase Your Technical Expertise
Prepare to discuss your experience with technical documentation and Quality Management Systems (QMS). Bring specific examples of how you've assessed compliance or managed certification activities in previous roles to demonstrate your hands-on experience.
✨Highlight Collaboration Skills
Since this role involves working with international clients and teams, be ready to share examples of how you've successfully collaborated across different regions. Emphasise your communication skills and adaptability in diverse environments.
✨Ask Insightful Questions
Prepare thoughtful questions about the company's portfolio and their approach to compliance. This not only shows your interest in the role but also gives you a chance to assess if the company aligns with your career goals.
