Regulatory & Quality Assurance Specialist (Medical Devices) in London
Regulatory & Quality Assurance Specialist (Medical Devices)

Regulatory & Quality Assurance Specialist (Medical Devices) in London

London Full-Time 35000 - 42000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Support compliance for medical devices and maintain Quality Management Systems.
  • Company: Join a leading consortium in clinical research and innovation.
  • Benefits: Gain valuable experience in a dynamic field with growth potential.
  • Other info: Strong organisational and communication skills are key to success.
  • Why this job: Make a difference in healthcare by ensuring quality and safety standards.
  • Qualifications: Bachelor’s degree in Life Sciences and 2 years in Regulatory Affairs or Quality Assurance.

The predicted salary is between 35000 - 42000 £ per year.

The Consortium for Clinical Research and Innovation Singapore is looking for a Regulatory Affairs professional in Greater London. The role involves supporting compliance with regulatory activities for medical devices and IVDs, maintaining the Quality Management System, and ensuring adherence to relevant standards like ISO 13485.

The ideal candidate will have a Bachelor’s degree in Life Sciences or a related field, with at least 2 years of experience in Regulatory Affairs or Quality Assurance. Strong organizational and communication skills are essential for success in this position.

Regulatory & Quality Assurance Specialist (Medical Devices) in London employer: Consortium for Clinical Research and Innovation Singapore

The Consortium for Clinical Research and Innovation Singapore is an exceptional employer, offering a dynamic work environment in Greater London that fosters innovation and collaboration in the medical devices sector. Employees benefit from a strong commitment to professional development, with opportunities for growth in Regulatory Affairs and Quality Assurance, while enjoying a supportive culture that values compliance and quality excellence.
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Contact Detail:

Consortium for Clinical Research and Innovation Singapore Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Regulatory & Quality Assurance Specialist (Medical Devices) in London

✨Tip Number 1

Network like a pro! Reach out to professionals in the Regulatory Affairs and Quality Assurance fields on LinkedIn. Join relevant groups and participate in discussions to get your name out there and show your expertise.

✨Tip Number 2

Prepare for interviews by brushing up on your knowledge of ISO 13485 and other relevant standards. We recommend creating a cheat sheet with key points to discuss, so you can confidently showcase your understanding during the interview.

✨Tip Number 3

Don’t just apply and wait! Follow up on your applications after a week or two. A quick email expressing your continued interest can set you apart from other candidates and shows your enthusiasm for the role.

✨Tip Number 4

Utilise our website to find job openings that match your skills. We’ve got a range of opportunities in Regulatory Affairs and Quality Assurance, so make sure to check back regularly and apply directly through us for the best chance!

We think you need these skills to ace Regulatory & Quality Assurance Specialist (Medical Devices) in London

Regulatory Affairs
Quality Assurance
ISO 13485
Compliance Management
Quality Management System
Organisational Skills
Communication Skills
Life Sciences Knowledge
Medical Device Regulations
IVD Regulations
Attention to Detail
Problem-Solving Skills
Team Collaboration
Analytical Skills

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights your experience in Regulatory Affairs and Quality Assurance, especially in the medical devices sector. We want to see how your background aligns with the role, so don’t be shy about showcasing relevant projects or achievements!

Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about regulatory compliance and quality management. We love seeing candidates who can communicate their enthusiasm for the field and how they can contribute to our team.

Showcase Your Skills: Don’t forget to highlight your organisational and communication skills in your application. These are key for success in this role, so give us examples of how you’ve used these skills in past positions or projects.

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 the role. Plus, it gives you a chance to explore more about what we do at StudySmarter!

How to prepare for a job interview at Consortium for Clinical Research and Innovation Singapore

✨Know Your Regulations

Make sure you brush up on the key regulations and standards relevant to medical devices, especially ISO 13485. Being able to discuss these in detail will show your expertise and commitment to compliance.

✨Showcase Your Experience

Prepare specific examples from your past roles that highlight your experience in Regulatory Affairs or Quality Assurance. Use the STAR method (Situation, Task, Action, Result) to structure your answers and make them impactful.

✨Demonstrate Organisational Skills

Since strong organisational skills are crucial for this role, be ready to discuss how you manage multiple projects or tasks. Share tools or methods you use to stay organised and ensure compliance with regulatory requirements.

✨Communicate Clearly

Effective communication is key in this position. Practice articulating complex regulatory concepts in a simple way. This will not only help you during the interview but also demonstrate your ability to convey important information to stakeholders.

Regulatory & Quality Assurance Specialist (Medical Devices) in London
Consortium for Clinical Research and Innovation Singapore
Location: London

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