Global Regulatory Affairs Associate, Medical Devices (UK)
Global Regulatory Affairs Associate, Medical Devices (UK)

Global Regulatory Affairs Associate, Medical Devices (UK)

Bachelor 36000 - 60000 Β£ / year (est.) No home office possible
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At a Glance

  • Tasks: Manage compliance with FDA and international regulations for medical devices.
  • Company: Leading regulatory consultancy in the UK with a strong reputation.
  • Benefits: Competitive salary, professional development, and a supportive work environment.
  • Why this job: Join a dynamic team and make a difference in the medical device industry.
  • Qualifications: Bachelor's degree and 4+ years' experience in regulatory affairs.
  • Other info: Opportunity for career advancement in a growing field.

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

A leading regulatory consultancy in the United Kingdom is seeking an experienced Regulatory Affairs professional to manage compliance with FDA and international regulations. The ideal candidate will have a Bachelor's degree and a minimum of 4 years' experience in the medical device sector.

Responsibilities include:

  • Conducting regulatory impact assessments
  • Managing annual registrations
  • Preparing FDA dossiers

Candidates must have excellent communication skills and be fluent in English.

Global Regulatory Affairs Associate, Medical Devices (UK) employer: Resourcing Life Science

As a leading regulatory consultancy in the UK, we pride ourselves on fostering a collaborative and innovative work culture that empowers our employees to excel in their roles. With a strong focus on professional development, we offer numerous growth opportunities and support for continuous learning, ensuring that our team remains at the forefront of the medical device sector. Our commitment to work-life balance and employee well-being makes us an exceptional employer for those seeking meaningful and rewarding careers in regulatory affairs.
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Contact Detail:

Resourcing Life Science Recruiting Team

StudySmarter Expert Advice 🀫

We think this is how you could land Global Regulatory Affairs Associate, Medical Devices (UK)

✨Tip Number 1

Network like a pro! Reach out to professionals in the regulatory affairs field, especially those in medical devices. LinkedIn is a great place to connect and engage with industry experts who might just have the inside scoop on job openings.

✨Tip Number 2

Prepare for interviews by brushing up on your knowledge of FDA regulations and international compliance standards. We recommend creating a cheat sheet of key points to discuss, so you can confidently showcase your expertise during the interview.

✨Tip Number 3

Don’t underestimate the power of follow-ups! After an interview, send a thank-you email to express your appreciation and reiterate your interest in the role. It’s a simple gesture that can set you apart from other candidates.

✨Tip Number 4

Apply through our website for the best chance at landing that Global Regulatory Affairs Associate position. We make it easy for you to showcase your skills and experience directly to hiring managers who are looking for someone just like you!

We think you need these skills to ace Global Regulatory Affairs Associate, Medical Devices (UK)

Regulatory Affairs
Compliance Management
FDA Regulations
International Regulations
Regulatory Impact Assessments
Annual Registrations
Dossier Preparation
Communication Skills
Medical Device Sector Experience
Bachelor's Degree
Fluency in English

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 background aligns with the 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 the perfect fit for this role and how your skills can help us manage compliance with FDA and international regulations.

Showcase Your Communication Skills: Since excellent communication is key for this role, make sure your application reflects that. Use clear and concise language, and don’t hesitate to demonstrate your fluency in English throughout your written materials.

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 Resourcing Life Science

✨Know Your Regulations

Make sure you brush up on the latest FDA and international regulations related to medical devices. Being able to discuss specific compliance issues or recent changes in the law will show that you're not just familiar with the basics, but that you’re genuinely engaged with the field.

✨Prepare Your Success Stories

Think of concrete examples from your past experience where you successfully managed regulatory impact assessments or prepared FDA dossiers. Use the STAR method (Situation, Task, Action, Result) to structure your answers, making it easy for the interviewer to see your capabilities in action.

✨Show Off Your Communication Skills

Since excellent communication is key for this role, practice articulating complex regulatory concepts in a clear and concise manner. You might even want to prepare a brief presentation on a relevant topic to demonstrate your ability to convey information effectively.

✨Ask Insightful Questions

Prepare thoughtful questions about the company’s approach to regulatory affairs and how they handle compliance challenges. This not only shows your interest in the role but also gives you a chance to assess if the company aligns with your career goals.

Global Regulatory Affairs Associate, Medical Devices (UK)
Resourcing Life Science
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