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For Companies At a Glance
- Tasks: Conduct regulatory assessments and manage submissions for medical devices.
- Company: Leading medical device company focused on innovation and compliance.
- Benefits: Competitive salary, health benefits, and opportunities for professional growth.
- Why this job: Join a dynamic team and make a difference in global healthcare regulations.
- Qualifications: Bachelor's degree and 4+ years in Regulatory Affairs with medical devices.
- Other info: Collaborative environment with a focus on career advancement.
The predicted salary is between 36000 - 60000 £ per year.
What to Expect
- Conduct regulatory impact assessments for product changes, including determination of letter-to-file versus submission requirements.
- Manage annual registrations, license renewals, and ongoing regulatory notifications.
- Support the preparation, submission, and maintenance of FDA dossiers and related technical documentation.
- Coordinate the collection, review, and consolidation of data for international regulatory registrations.
- Collaborate with global Regulatory Affairs partners and cross-functional stakeholders to ensure timely, compliant submissions.
- Execute administrative, documentation, and procedural activities supporting the Regulatory Affairs function.
Requirements
- Bachelor degree
- Min 4 years of experience in Regulatory Affairs in the medical device
- Proven experience with global submissions, preferably including FDA
- Excellent communication and problem-solving skills
- Fluent in English (written and spoken).
Regulatory Affairs Associate – Medical Device United Kingdom employer: Resourcing Life Science
Contact Detail:
Resourcing Life Science Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Regulatory Affairs Associate – Medical Device United Kingdom
✨Tip Number 1
Network like a pro! Reach out to professionals in the Regulatory Affairs field, especially those who work with medical devices. Use platforms like LinkedIn to connect and engage with them; you never know who might have a lead on your dream job!
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of FDA submissions and regulatory requirements. We recommend creating a list of common interview questions related to your experience and practicing your answers. Confidence is key!
✨Tip Number 3
Don’t just apply anywhere—focus on companies that align with your values and career goals. When you find a role that excites you, apply through our website for a smoother process and to show your genuine interest!
✨Tip Number 4
Follow up after interviews! A quick thank-you email can go a long way in leaving a positive impression. It shows your enthusiasm for the role and keeps you fresh in their minds as they make their decision.
We think you need these skills to ace Regulatory Affairs Associate – Medical Device United Kingdom
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Regulatory Affairs Associate role. Highlight your experience in managing registrations and submissions, especially with FDA dossiers, as this will show us you’ve got the right background for the job.
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about regulatory affairs in the medical device sector and how your skills align with our needs. We love seeing genuine enthusiasm!
Showcase Your Communication Skills: Since excellent communication is key in this role, make sure your application reflects that. Use clear, concise language and structure your documents well. This will give us a taste of how you’ll communicate with stakeholders.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the easiest way for us to receive your application and ensures you’re considered for the role. Plus, it gives you a chance to explore more about us!
How to prepare for a job interview at Resourcing Life Science
✨Know Your Regulations
Make sure you brush up on the latest regulations and guidelines related to medical devices, especially those from the FDA. Being able to discuss specific regulatory requirements and how they impact product changes will show your expertise and readiness for the role.
✨Prepare Real-Life Examples
Think of specific instances from your past experience where you've successfully managed submissions or navigated regulatory challenges. Use the STAR method (Situation, Task, Action, Result) to structure your answers, as this will help you convey your problem-solving skills effectively.
✨Showcase Your Communication Skills
Since collaboration with global partners and cross-functional teams is key, be prepared to demonstrate your communication style. Practice explaining complex regulatory concepts in simple terms, as this will highlight your ability to work well with diverse stakeholders.
✨Ask Insightful Questions
At the end of the interview, have a few thoughtful questions ready about the company's regulatory processes or upcoming projects. 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.
