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- Tasks: Monitor regulations, ensure compliance, and support product lifecycle quality.
- Company: Dynamic organisation focused on global compliance in medical devices.
- Benefits: Impactful work, collaboration with diverse teams, and opportunities for innovation.
- Why this job: Make a real difference to patients and products while shaping world-class compliance.
- Qualifications: Passion for quality and problem-solving skills.
- Other info: Join a vibrant team dedicated to continuous improvement and innovation.
The predicted salary is between 28800 - 48000 £ per year.
Do you thrive on Quality, standards, audits, and the challenge of keeping products compliant in a fast‑moving global landscape? If you’re energised by solving problems, spotting gaps, and helping teams deliver their best, this is an opportunity to play a pivotal role at the heart of our Quality organisation.
What you’ll be doing:
- Monitoring new and evolving regulations and standards, assessing their impact on our products and Quality Management System.
- Ensuring ongoing compliance by reviewing regulatory updates and aligning product claims, documentation, and processes.
- Supporting compliance across the full product lifecycle — from early design and development through manufacturing and post‑market surveillance.
- Identifying gaps in regulatory and standards compliance, coordinating cross‑functional actions, and driving timely closure.
- Tracking and trending key quality and compliance activities, providing clear visibility of risks and progress to leadership.
- Working with major global regulatory frameworks including EU MDR, ISO 13485, FDA 21 CFR Part 820/QMSR, Japan MHLW Ordinance 169, and other international requirements.
Why this role matters:
You’ll be at the centre of global compliance, helping ensure our medical devices are safe, effective, and ready for markets worldwide. Your work will directly influence continuous improvement, strengthen our Quality System, and support teams across the organisation.
Why you’ll love it:
- Your contribution genuinely makes a difference to patients and products.
- You’ll collaborate with a wide range of teams, technologies, and markets.
- You’ll be part of a dynamic Quality function where compliance, improvement, and innovation come together.
If you’re passionate about Quality and excited by the idea of shaping world‑class compliance, we’d love to welcome you to the team.
Quality Compliance Specialist in Renfrew employer: Terumo Aortic
Contact Detail:
Terumo Aortic Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Quality Compliance Specialist in Renfrew
✨Tip Number 1
Network like a pro! Reach out to people in the industry, attend events, and connect on LinkedIn. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by researching the company and its compliance practices. Show us that you understand the regulatory landscape and how it impacts their products. Tailor your answers to highlight your problem-solving skills and attention to detail.
✨Tip Number 3
Follow up after interviews! A quick thank-you email can go a long way. It shows your enthusiasm for the role and keeps you fresh in their minds. Plus, it’s a great chance to reiterate why you’re the perfect fit for the Quality Compliance Specialist position.
✨Tip Number 4
Don’t forget to apply through our website! We love seeing applications come directly from candidates who are genuinely interested in joining our team. It gives us a better sense of your commitment to being part of our Quality organisation.
We think you need these skills to ace Quality Compliance Specialist in Renfrew
Some tips for your application 🫡
Tailor Your CV: Make sure your CV reflects the skills and experiences that align with the Quality Compliance Specialist role. Highlight any relevant experience with regulations, standards, and compliance processes to show us you’re the right fit.
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to tell us why you’re passionate about quality and compliance. Share specific examples of how you've tackled challenges in previous roles to demonstrate your problem-solving skills.
Showcase Your Knowledge: We want to see that you’re up-to-date with the latest regulations and standards. Mention any relevant certifications or training you’ve completed, especially those related to EU MDR, ISO 13485, or FDA guidelines.
Apply Through Our Website: Don’t forget to submit your application through our website! It’s the best way for us to receive your details and ensures you’re considered for the role. Plus, it makes the whole process smoother for everyone involved.
How to prepare for a job interview at Terumo Aortic
✨Know Your Regulations
Familiarise yourself with key regulations like EU MDR, ISO 13485, and FDA 21 CFR Part 820. Being able to discuss these frameworks confidently will show that you understand the compliance landscape and are ready to tackle the challenges of the role.
✨Showcase Problem-Solving Skills
Prepare examples of how you've identified gaps in compliance or quality standards in previous roles. Highlighting your problem-solving abilities will demonstrate your proactive approach and readiness to contribute to the team.
✨Understand the Product Lifecycle
Brush up on the full product lifecycle from design to post-market surveillance. Being able to articulate how compliance fits into each stage will impress interviewers and show that you can support teams effectively throughout the process.
✨Communicate Clearly
Practice explaining complex compliance concepts in simple terms. Clear communication is key in this role, so being able to convey your thoughts succinctly will help you stand out as a candidate who can bridge gaps between technical and non-technical teams.
