Global Regulatory Affairs Specialist – Medical Devices in London
Global Regulatory Affairs Specialist – Medical Devices

Global Regulatory Affairs Specialist – Medical Devices in London

London Full-Time 30000 - 42000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Ensure medical devices meet global regulatory standards and manage submissions.
  • Company: International medical devices company with a strong team culture.
  • Benefits: Competitive salary, attractive benefits, and a supportive work environment.
  • Why this job: Join a dynamic team and make a difference in healthcare compliance.
  • Qualifications: Bachelor's degree and 2-5 years in Medical Devices Regulatory.
  • Other info: Engaging workplace with opportunities for professional growth.

The predicted salary is between 30000 - 42000 £ per year.

An international medical devices company in the UK is seeking a Regulatory Affairs Specialist. The successful candidate will be responsible for ensuring regulatory products comply with specific country requirements.

Key responsibilities include:

  • Managing global regulatory submissions
  • Liaising with regulatory authorities

Ideal candidates will have a relevant Bachelor's degree and 2-5 years of experience in Medical Devices Regulatory. The company offers a competitive salary and attractive benefits, promoting a culture of engagement and team spirit.

Global Regulatory Affairs Specialist – Medical Devices in London employer: Biocomposites

Join a leading international medical devices company in the UK, where we prioritise employee engagement and foster a collaborative work culture. With competitive salaries and attractive benefits, we are committed to your professional growth, offering opportunities to develop your skills in a dynamic environment that values innovation and teamwork.
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Contact Detail:

Biocomposites Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Global Regulatory Affairs Specialist – Medical Devices in London

Tip Number 1

Network like a pro! Reach out to professionals in the medical devices field on LinkedIn. Join relevant groups and engage in discussions to get your name out there and learn about potential job openings.

Tip Number 2

Prepare for interviews by brushing up on your knowledge of global regulatory requirements. We recommend creating a cheat sheet of key regulations and recent changes in the industry to impress your interviewers.

Tip Number 3

Don’t just apply anywhere; focus on companies that align with your values and career goals. Use our website to find roles that excite you and match your skills, making your application stand out.

Tip Number 4

Follow up after interviews! A quick thank-you email can go a long way in showing your enthusiasm for the role. It keeps you fresh in their minds and demonstrates your professionalism.

We think you need these skills to ace Global Regulatory Affairs Specialist – Medical Devices in London

Regulatory Compliance
Global Regulatory Submissions
Liaising with Regulatory Authorities
Medical Devices Knowledge
Bachelor's Degree in a Relevant Field
2-5 Years of Experience in Regulatory Affairs
Attention to Detail
Communication Skills
Team Collaboration
Problem-Solving Skills

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights your experience in Medical Devices Regulatory. 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 affairs and how your skills can help us navigate the complexities of global submissions.

Showcase Your Communication Skills: As a Regulatory Affairs Specialist, you'll be liaising with authorities. Make sure your application reflects your ability to communicate clearly and effectively, both in writing and verbally.

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!

How to prepare for a job interview at Biocomposites

Know Your Regulations

Make sure you brush up on the specific regulations related to medical devices in the countries relevant to the role. Understanding the nuances of these regulations will not only impress your interviewers but also show that you're serious about compliance.

Showcase Your Experience

Prepare to discuss your previous experience in regulatory affairs, especially any global submissions you've managed. Use specific examples to highlight your problem-solving skills and how you've successfully navigated complex regulatory environments.

Engage with the Interviewers

Don’t just answer questions; engage with your interviewers. Ask insightful questions about their current projects or challenges they face in regulatory affairs. This shows your genuine interest in the role and helps you assess if the company is the right fit for you.

Demonstrate Team Spirit

Since the company promotes a culture of engagement and team spirit, be ready to discuss how you’ve collaborated with cross-functional teams in the past. Share examples that illustrate your ability to work well with others and contribute positively to a team environment.

Global Regulatory Affairs Specialist – Medical Devices in London
Biocomposites
Location: London
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  • Global Regulatory Affairs Specialist – Medical Devices in London

    London
    Full-Time
    30000 - 42000 £ / year (est.)
  • B

    Biocomposites

    50-100
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