Global Regulatory Affairs Specialist – Medical Devices
Global Regulatory Affairs Specialist – Medical Devices

Global Regulatory Affairs Specialist – Medical Devices

Full-Time 30000 - 50000 £ / 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 - 50000 £ 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 employer: Biocomposites

Join a leading international medical devices company in the UK, where you will thrive in a collaborative and engaging work culture that values team spirit and innovation. With competitive salaries and attractive benefits, we are committed to your professional growth, offering ample opportunities for development in the dynamic field of regulatory affairs. Experience the unique advantage of working in a sector that directly impacts healthcare and patient outcomes, making your role both meaningful and rewarding.
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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

Tip Number 1

Network like a pro! Reach out to professionals in the medical devices field on LinkedIn or at industry events. We can’t stress enough how valuable personal connections can be in landing that dream job.

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

Showcase your experience with real-life examples during interviews. We all love a good story, so share specific instances where you successfully managed regulatory submissions or liaised with authorities.

Tip Number 4

Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we’re always looking for passionate candidates who fit our culture of engagement and team spirit.

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

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 Medical Devices Regulatory
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 key responsibilities mentioned in the job description.

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 you can contribute to our team. Keep it engaging and relevant to the role.

Showcase Your Experience: When detailing your experience, focus on specific projects or submissions you've managed. We love seeing concrete examples of how you've navigated regulatory requirements in the past.

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 regulatory requirements for medical devices in various countries. Familiarise yourself with the latest guidelines and standards, as this will show your potential employer that you're proactive and knowledgeable about the field.

Showcase Your Experience

Prepare to discuss your previous roles in regulatory affairs, especially any experience you have with global submissions. Use specific examples to highlight how you've successfully navigated complex regulatory landscapes, as this will demonstrate your capability and confidence.

Engage with the Interviewers

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

Emphasise Team Spirit

Since the company values team spirit, be ready to discuss how you’ve collaborated with others in past roles. Share examples of how you’ve worked effectively within a team to achieve regulatory goals, as this aligns with their culture of engagement.

Global Regulatory Affairs Specialist – Medical Devices
Biocomposites
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  • Global Regulatory Affairs Specialist – Medical Devices

    Full-Time
    30000 - 50000 £ / year (est.)
  • B

    Biocomposites

    50-100
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