Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- Tasks: Ensure medical devices meet quality standards and regulatory guidelines.
- Company: Leading consultancy in medical device development based in Bristol.
- Benefits: Competitive salary, professional growth, and the chance to work with top pharmaceutical clients.
- Why this job: Make a real difference in healthcare by influencing life-changing technologies.
- Qualifications: Degree in relevant field and experience in quality assurance.
- Other info: Join a dynamic team dedicated to innovation in medical devices.
The predicted salary is between 36000 - 60000 £ per year.
A consultancy in medical device development in Bristol is seeking a Quality & Regulatory Engineer passionate about ensuring device development aligns with latest guidelines. The role involves maintaining the ISO-certified QMS, supporting audits, and contributing to risk management.
Ideal candidates will possess:
- a good degree in a relevant discipline
- extensive experience in quality assurance
- strong analytical skills
This position offers the opportunity to work with top pharmaceutical clients and influence the development of life-changing healthcare technologies.
Global Medical Device Quality & Regulatory Engineer in Bristol employer: Crux Product Design
Contact Detail:
Crux Product Design Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Global Medical Device Quality & Regulatory Engineer in Bristol
✨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 Quality & Regulatory Engineer role.
✨Tip Number 2
Prepare for interviews by brushing up on ISO standards and regulatory guidelines. We recommend practising common interview questions related to quality assurance and risk management, so you can showcase your analytical skills with confidence.
✨Tip Number 3
Don’t just apply anywhere; focus on companies that align with your passion for healthcare technology. Use our website to find roles that excite you, and tailor your approach to show how you can contribute to their mission.
✨Tip Number 4
Follow up after interviews! A quick thank-you email can set you apart from other candidates. We believe it shows your enthusiasm for the role and keeps you fresh in the interviewer’s mind.
We think you need these skills to ace Global Medical Device Quality & Regulatory Engineer in Bristol
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience in quality assurance and regulatory compliance. We want to see how your background aligns with the role, so don’t be shy about showcasing your relevant skills and achievements!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to express your passion for medical device development and how you can contribute to our ISO-certified QMS. Let us know why you’re excited about working with top pharmaceutical clients.
Showcase Your Analytical Skills: Since strong analytical skills are key for this role, make sure to include examples of how you've used these skills in past positions. We love seeing concrete examples that demonstrate your problem-solving abilities!
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for this exciting opportunity. Don’t miss out on the chance to influence life-changing healthcare technologies!
How to prepare for a job interview at Crux Product Design
✨Know Your Standards
Familiarise yourself with the latest ISO standards and regulations relevant to medical devices. Being able to discuss how you’ve applied these in past roles will show your expertise and passion for quality assurance.
✨Showcase Your Analytical Skills
Prepare examples that highlight your analytical skills, especially in risk management and quality control. Use specific scenarios where you identified issues and implemented solutions to demonstrate your problem-solving abilities.
✨Research the Company
Dive into the consultancy’s recent projects and their approach to medical device development. This knowledge will not only help you tailor your answers but also show your genuine interest in their work and how you can contribute.
✨Prepare for Scenario Questions
Expect questions that assess your response to real-world challenges in quality and regulatory environments. Practise articulating your thought process and decision-making in these scenarios to convey confidence and competence.
