Regulatory Lead – Medical Devices (UKCA/CE) in Swindon
Regulatory Lead – Medical Devices (UKCA/CE)

Regulatory Lead – Medical Devices (UKCA/CE) in Swindon

Swindon Full-Time 50000 - 65000 £ / year (est.) No home office possible
Barrington James Limited

At a Glance

  • Tasks: Ensure compliance with UKCA and CE marking for Class I medical devices.
  • Company: Leading medical device manufacturer known for innovation.
  • Benefits: Opportunity to make an impact in a growing company.
  • Why this job: Join a dynamic team and contribute to innovative projects.
  • Qualifications: Experience in regulatory compliance and strong teamwork skills.
  • Other info: Apply quickly as recruitment may close early!

The predicted salary is between 50000 - 65000 £ per year.

A leading medical device manufacturer in the United Kingdom, England, is seeking a Regulatory Lead for Class I medical devices. This role involves ensuring compliance with UKCA and CE marking requirements and working cross-functionally with various teams to support product development and maintain compliant documentation.

This is a fantastic opportunity for an ambitious individual looking to make an impact in a growing company known for its innovative projects. Interested candidates should apply immediately as recruitment may close early.

Regulatory Lead – Medical Devices (UKCA/CE) in Swindon employer: Barrington James Limited

As a leading medical device manufacturer in the UK, we pride ourselves on fostering a dynamic work culture that encourages innovation and collaboration. Our employees benefit from comprehensive professional development opportunities, competitive remuneration, and a supportive environment that values their contributions. Join us in making a meaningful impact in the healthcare sector while enjoying the unique advantages of working in a forward-thinking company dedicated to excellence.
Barrington James Limited

Contact Detail:

Barrington James Limited Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Regulatory Lead – Medical Devices (UKCA/CE) in Swindon

Tip Number 1

Network like a pro! Reach out to professionals in the medical device industry on LinkedIn or at local events. We all know that sometimes it’s not just what you know, but who you know that can help you land that Regulatory Lead role.

Tip Number 2

Prepare for your interviews by brushing up on UKCA and CE marking requirements. We recommend creating a cheat sheet of key regulations and examples of how you've ensured compliance in past roles. This will show you're ready to hit the ground running!

Tip Number 3

Don’t forget to showcase your cross-functional collaboration skills! Think of specific projects where you worked with different teams. We want to see how you can bring people together to support product development in this role.

Tip Number 4

Apply through our website! It’s the quickest way to get your application in front of the right people. We’re excited to see your passion for regulatory affairs and how you can contribute to our innovative projects.

We think you need these skills to ace Regulatory Lead – Medical Devices (UKCA/CE) in Swindon

Regulatory Compliance
UKCA Marking
CE Marking
Cross-Functional Collaboration
Documentation Management
Product Development Support
Attention to Detail
Analytical Skills
Communication Skills
Project Management
Problem-Solving Skills
Knowledge of Medical Device Regulations
Adaptability
Teamwork

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights your experience with UKCA and CE marking requirements. 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 in medical devices and how you can contribute to our innovative projects. Keep it concise but impactful!

Showcase Cross-Functional Experience: Since this role involves working with various teams, make sure to mention any cross-functional collaboration you've been part of. We love seeing candidates who can work well with others to achieve common goals!

Apply Through Our Website: We encourage you to apply directly through our website for a smoother application process. It helps us keep track of your application and ensures you don’t miss out on this fantastic opportunity!

How to prepare for a job interview at Barrington James Limited

Know Your Regulations

Make sure you brush up on UKCA and CE marking requirements before the interview. Being able to discuss specific regulations and how they apply to Class I medical devices will show that you're not just familiar with the basics, but that you’re ready to dive into the details.

Show Your Cross-Functional Skills

This role involves working with various teams, so be prepared to share examples of how you've successfully collaborated in the past. Think about times when you’ve worked with product development or quality assurance teams and how you navigated any challenges.

Prepare for Scenario Questions

Expect questions that ask how you would handle specific regulatory challenges. Practise articulating your thought process and decision-making skills in these scenarios, as it will demonstrate your problem-solving abilities and regulatory knowledge.

Express Your Passion for Innovation

Since the company is known for its innovative projects, convey your enthusiasm for working in a dynamic environment. Share any relevant experiences where you contributed to innovative solutions in regulatory affairs or product development to highlight your fit for the role.

Regulatory Lead – Medical Devices (UKCA/CE) in Swindon
Barrington James Limited
Location: Swindon

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