Remote Regulatory Affairs Specialist (Medical Devices) in London
Remote Regulatory Affairs Specialist (Medical Devices)

Remote 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 compliance for medical devices and lead regulatory assessments.
  • Company: Global medical technology company focused on innovation.
  • Benefits: Flexible remote work, competitive salary, and opportunities for professional growth.
  • Why this job: Join a vibrant team and pioneer solutions that improve lives.
  • Qualifications: 1-2 years in regulatory affairs and relevant degree.
  • Other info: Dynamic environment with a focus on innovation and teamwork.

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

A global medical technology company is seeking a Regulatory Affairs Specialist to ensure compliance for its products. You will drive regulatory processes, submit documentation, and lead regulatory assessments.

The ideal candidate will have 1-2 years in regulatory affairs, a relevant degree, and experience with medical devices.

Join us to pioneer solutions that improve lives and work in a vibrant team focused on innovation.

Remote Regulatory Affairs Specialist (Medical Devices) in London employer: Convatec

Join a global leader in medical technology that prioritises innovation and employee development. As a Regulatory Affairs Specialist, you will thrive in a collaborative work culture that values your contributions and offers ample opportunities for professional growth. Enjoy the flexibility of remote work while being part of a team dedicated to pioneering solutions that enhance lives.
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Contact Detail:

Convatec Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Remote Regulatory Affairs Specialist (Medical Devices) in London

✨Tip Number 1

Network like a pro! Reach out to professionals in the regulatory affairs field, especially those working with medical devices. LinkedIn is a great place to start – connect, engage, and don’t be shy about asking for advice or insights.

✨Tip Number 2

Prepare for interviews by brushing up on your knowledge of regulatory processes and compliance standards. We recommend practising common interview questions related to medical devices and thinking of examples from your experience that showcase your skills.

✨Tip Number 3

Showcase your passion for innovation! During interviews, express your enthusiasm for improving lives through medical technology. Share any relevant projects or experiences that highlight your commitment to the field.

✨Tip Number 4

Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive and engaged with our company.

We think you need these skills to ace Remote Regulatory Affairs Specialist (Medical Devices) in London

Regulatory Compliance
Documentation Submission
Regulatory Assessments
Medical Device Knowledge
Analytical Skills
Attention to Detail
Communication Skills
Team Collaboration
Problem-Solving Skills
Project Management
Innovation Mindset
Relevant Degree in Life Sciences or Engineering

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights your experience in regulatory affairs, especially with medical devices. We want to see how your skills align 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 you can contribute to our mission of improving lives through innovative solutions. Keep it concise but impactful!

Showcase Your Knowledge: In your application, demonstrate your understanding of regulatory processes and compliance standards. We love candidates who can speak our language, so include any specific regulations or guidelines you’re familiar with that relate to medical devices.

Apply Through Our Website: We encourage you to apply directly through our website for a smoother process. It helps us keep track of applications and ensures you’re considered for the role. Plus, it’s super easy to do!

How to prepare for a job interview at Convatec

✨Know Your Regulations

Make sure you brush up on the key regulations and standards related to medical devices. Familiarise yourself with the specific compliance requirements that the company adheres to, as this will show your commitment and understanding of the role.

✨Showcase Your Experience

Prepare to discuss your previous experience in regulatory affairs, especially any hands-on work with medical devices. Be ready to share specific examples of how you've navigated regulatory processes or submitted documentation successfully.

✨Ask Insightful Questions

Come prepared with questions that demonstrate your interest in the company's products and regulatory strategies. This not only shows your enthusiasm but also helps you gauge if the company aligns with your career goals.

✨Highlight Your Team Spirit

Since the role involves working within a vibrant team, be sure to express your collaborative skills. Share examples of how you've worked effectively in teams before, particularly in high-pressure situations or during regulatory assessments.

Remote Regulatory Affairs Specialist (Medical Devices) in London
Convatec
Location: London

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