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- Tasks: Support new product developments and create submissions for regulatory compliance.
- Company: Join a leading multi-national medical device organisation making a difference in healthcare.
- Benefits: Enjoy hybrid or remote work options, competitive salary, bonuses, and company perks.
- Why this job: Engage in varied tasks within a dynamic environment that challenges and develops your skills.
- Qualifications: 2+ years in a similar role with knowledge of EU MDR & 510(k) requirements.
- Other info: Immediate start available; apply now to be part of an innovative team!
The predicted salary is between 24000 - 32000 £ per year.
I am currently recruiting for a Regulatory Affairs Associate to work for a multi-national medical device organisation. Salary up to £40,000 pa + benefits.
On a day-to-day basis, you can expect to be supporting new product developments and creation of their submissions in Europe and USA in compliance with regulatory requirements.
Essential Requirements:
- 2+ years within a similar position
- Working knowledge of regulatory requirements
- Ideally has experience in key market approval requirements within Europe and USA (EU MDR & 510(k))
- Understanding of Risk Management within a Medical Device industry
This is a fantastic opportunity for a Regulatory Affairs Associate to work for a leader within their field where the work is continuously varied keeping you engaged and challenged.
This is an immediate requirement so if you have the required skills and experience then please get in touch ASAP with an up to date copy of your CV.
Either apply direct or contact David on 01183 366 100.
Regulatory Affairs Associate (Hybrid/Remote) employer: Avd Appoint
Contact Detail:
Avd Appoint Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Regulatory Affairs Associate (Hybrid/Remote)
✨Tip Number 1
Familiarise yourself with the latest EU MDR and 510(k) requirements. Being well-versed in these regulations will not only boost your confidence during interviews but also demonstrate your commitment to the role.
✨Tip Number 2
Network with professionals in the regulatory affairs field, especially those who have experience in medical devices. Engaging with industry experts can provide you with valuable insights and potentially lead to referrals.
✨Tip Number 3
Prepare to discuss specific examples of how you've navigated regulatory challenges in your previous roles. This will showcase your problem-solving skills and practical knowledge, making you a standout candidate.
✨Tip Number 4
Stay updated on current trends and changes in the regulatory landscape for medical devices. Showing that you are proactive about your professional development can impress potential employers and set you apart from other candidates.
We think you need these skills to ace Regulatory Affairs Associate (Hybrid/Remote)
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your relevant experience in regulatory affairs, particularly focusing on your knowledge of EU MDR and 510(k) requirements. Use specific examples to demonstrate your skills and achievements in previous roles.
Craft a Compelling Cover Letter: Write a cover letter that not only outlines your qualifications but also expresses your enthusiasm for the role. Mention why you are interested in working for a multi-national medical device organisation and how your background aligns with their needs.
Highlight Relevant Experience: In your application, emphasise your 2+ years of experience in regulatory affairs. Discuss any specific projects or submissions you have worked on that relate to new product developments and compliance with regulatory requirements.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any spelling or grammatical errors. A polished application reflects your attention to detail, which is crucial in regulatory affairs.
How to prepare for a job interview at Avd Appoint
✨Know Your Regulations
Make sure you have a solid understanding of the regulatory requirements for medical devices, especially EU MDR and 510(k) processes. Brush up on any recent changes or updates in these regulations to demonstrate your knowledge during the interview.
✨Showcase Relevant Experience
Prepare to discuss your previous roles and how they relate to the position. Highlight specific projects where you supported product development or submissions, and be ready to explain your contributions and the outcomes.
✨Understand Risk Management
Since risk management is crucial in the medical device industry, be prepared to talk about your experience with risk assessments and how you've applied risk management principles in your past roles.
✨Ask Insightful Questions
Prepare thoughtful questions about the company's products, their regulatory strategies, and the team you'll be working with. This shows your genuine interest in the role and helps you assess if the company is the right fit for you.
