Global Regulatory Affairs Lead – Medical Devices in Yarnton
Global Regulatory Affairs Lead – Medical Devices

Global Regulatory Affairs Lead – Medical Devices in Yarnton

Yarnton Full-Time 43200 - 72000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Lead regulatory clearances for medical devices in global markets.
  • Company: Leading technology firm in the UK with a focus on innovation.
  • Benefits: Competitive salary, flexible working options, and career advancement opportunities.
  • Why this job: Shape regulatory strategies and ensure compliance in a cutting-edge tech environment.
  • Qualifications: 5+ years of compliance experience in medical devices and knowledge of EU/FDA regulations.
  • Other info: Join a dynamic team and make a real impact in the healthcare technology sector.

The predicted salary is between 43200 - 72000 £ per year.

A leading technology firm in the United Kingdom is seeking a Regulatory Affairs Manager to oversee regulatory clearances in global markets. The ideal candidate will have over 5 years of compliance experience in the medical device sector and a strong knowledge of EU and FDA regulations. This role offers an opportunity to contribute directly to the regulatory strategy and ensure compliance across products in a cutting-edge technology environment.

Global Regulatory Affairs Lead – Medical Devices in Yarnton employer: Vicon

As a leading technology firm in the United Kingdom, we pride ourselves on fostering a dynamic work culture that encourages innovation and collaboration. Our employees benefit from comprehensive professional development opportunities, competitive compensation packages, and a commitment to work-life balance, all while contributing to groundbreaking advancements in the medical device sector. Join us to be part of a team that values your expertise and empowers you to make a meaningful impact in global regulatory affairs.
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Contact Detail:

Vicon Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Global Regulatory Affairs Lead – Medical Devices in Yarnton

Tip Number 1

Network like a pro! Reach out to professionals in the medical device sector 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 EU and FDA regulations. We recommend creating a cheat sheet of key points to discuss, so you can showcase your expertise and confidence during the interview.

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 and match your skills in regulatory affairs.

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 and professionalism, which are key in the regulatory field.

We think you need these skills to ace Global Regulatory Affairs Lead – Medical Devices in Yarnton

Regulatory Compliance
Knowledge of EU Regulations
Knowledge of FDA Regulations
Medical Device Sector Experience
Regulatory Strategy Development
Project Management
Stakeholder Engagement
Analytical Skills
Attention to Detail
Communication Skills
Problem-Solving Skills
Adaptability
Technical Aptitude

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights your experience in regulatory affairs, especially in the medical device sector. We want to see how your skills align with the requirements 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 the perfect fit for the Global Regulatory Affairs Lead role. Share specific examples of your compliance experience and knowledge of EU and FDA regulations.

Showcase Your Achievements: Don’t just list your responsibilities; highlight your achievements in previous roles. We love to see how you've contributed to regulatory strategies or improved compliance processes in your past positions.

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 in our cutting-edge technology environment.

How to prepare for a job interview at Vicon

Know Your Regulations

Make sure you brush up on EU and FDA regulations before the interview. Being able to discuss specific compliance scenarios and how you've navigated regulatory challenges in the past will show that you're not just familiar with the rules, but that you can apply them effectively.

Showcase Your Experience

Prepare to share concrete examples from your 5+ years in the medical device sector. Highlight projects where you successfully led regulatory clearances or contributed to a regulatory strategy. This will demonstrate your hands-on experience and ability to drive results.

Understand the Company’s Products

Research the technology firm and its product offerings. Understanding their portfolio will allow you to tailor your responses and show how your expertise aligns with their needs. It also shows genuine interest in the role and the company.

Ask Insightful Questions

Prepare thoughtful questions about the company's regulatory strategy and future challenges they might face in global markets. This not only shows your enthusiasm for the role but also your strategic thinking and understanding of the industry landscape.

Global Regulatory Affairs Lead – Medical Devices in Yarnton
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Location: Yarnton

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  • Global Regulatory Affairs Lead – Medical Devices in Yarnton

    Yarnton
    Full-Time
    43200 - 72000 £ / year (est.)
  • V

    Vicon

    50-100
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