Global Regulatory Affairs Officer - IVD/Medtech in Edinburgh
Global Regulatory Affairs Officer - IVD/Medtech

Global Regulatory Affairs Officer - IVD/Medtech in Edinburgh

Edinburgh Full-Time 36000 - 60000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Manage global product license registrations and ensure compliance with industry standards.
  • Company: Leading medical device company based in Edinburgh with a strong reputation.
  • Benefits: Full-time role with potential relocation support and career advancement opportunities.
  • Why this job: Join a dynamic team and make a difference in the medical device industry.
  • Qualifications: Experience in regulatory affairs and a degree in a related field required.
  • Other info: Exciting opportunity to work in a fast-paced environment with global impact.

The predicted salary is between 36000 - 60000 £ per year.

A leading medical device company in Edinburgh is looking for a Regulatory Affairs Officer to manage product license registrations globally.

Key responsibilities include:

  • Preparing regulatory submissions
  • Advising project teams on requirements
  • Ensuring compliance with standards like ISO13485 and FDA regulations

The ideal candidate should have relevant experience in the medical device industry and possess a degree in regulatory affairs or a similar field. This full-time role may offer relocation support for the right candidate.

Global Regulatory Affairs Officer - IVD/Medtech in Edinburgh employer: Jobster

As a leading medical device company based in Edinburgh, we pride ourselves on fostering a collaborative and innovative work culture that empowers our employees to excel in their roles. We offer competitive benefits, including relocation support for the right candidate, and provide ample opportunities for professional growth and development within the dynamic field of regulatory affairs. Join us to make a meaningful impact in the healthcare sector while enjoying a supportive environment that values your contributions.
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Contact Detail:

Jobster Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Global Regulatory Affairs Officer - IVD/Medtech in Edinburgh

✨Tip Number 1

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

✨Tip Number 2

Prepare for interviews by brushing up on your knowledge of regulatory standards like ISO13485 and FDA regulations. We recommend practising common interview questions and having examples ready that showcase your experience in regulatory affairs.

✨Tip Number 3

Don’t just apply anywhere; focus on companies that align with your values and career goals. We suggest using our website to find roles that excite you, as we have tailored listings that match your skills and aspirations.

✨Tip Number 4

Follow up after interviews! A simple thank-you email can set you apart from other candidates. We believe it shows your enthusiasm for the role and keeps you fresh in the interviewer’s mind.

We think you need these skills to ace Global Regulatory Affairs Officer - IVD/Medtech in Edinburgh

Regulatory Submissions
ISO 13485
FDA Regulations
Compliance Management
Project Team Advising
Medical Device Industry Experience
Degree in Regulatory Affairs
Global Product Licensing

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights your experience in regulatory affairs, especially in the IVD/Medtech sector. We want to see how your background aligns with the key responsibilities mentioned in the job description.

Showcase Relevant Skills: Emphasise your knowledge of standards like ISO13485 and FDA regulations. We’re looking for candidates who can demonstrate their understanding of compliance requirements, so don’t hold back!

Craft a Compelling Cover Letter: Use your cover letter to tell us why you’re passionate about regulatory affairs and how your experience makes you a great fit for our team. We love seeing genuine enthusiasm and a clear connection to the role.

Apply Through Our Website: For the best chance of success, make sure to apply through our website. It’s the easiest way for us to keep track of your application and ensures you’re considered for the role!

How to prepare for a job interview at Jobster

✨Know Your Regulations

Make sure you brush up on key regulations like ISO13485 and FDA guidelines. Being able to discuss these standards confidently will show that you’re not just familiar with them, but that you can apply them in real-world scenarios.

✨Showcase Your Experience

Prepare specific examples from your past roles in the medical device industry. Highlight how you’ve successfully managed product license registrations or navigated complex regulatory submissions. This will demonstrate your hands-on experience and problem-solving skills.

✨Understand the Company’s Products

Do your homework on the company’s product line and any recent developments in their regulatory affairs. This knowledge will help you tailor your answers and show genuine interest in their work, making you a more appealing candidate.

✨Ask Insightful Questions

Prepare thoughtful questions about the company’s regulatory processes or challenges they face in the industry. This not only shows your enthusiasm for the role but also your critical thinking skills and willingness to engage in meaningful discussions.

Global Regulatory Affairs Officer - IVD/Medtech in Edinburgh
Jobster
Location: Edinburgh
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  • Global Regulatory Affairs Officer - IVD/Medtech in Edinburgh

    Edinburgh
    Full-Time
    36000 - 60000 £ / year (est.)
  • J

    Jobster

    50-100
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