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- Tasks: Support new product developments and create submissions for Europe and USA.
- Company: Join a leading multi-national medical device organisation making a real impact.
- Benefits: Enjoy hybrid or remote work, competitive salary, bonuses, and great company perks.
- Why this job: Engage in varied tasks within a dynamic environment that challenges and excites you.
- Qualifications: 2+ years in a similar role with knowledge of regulatory requirements.
- Other info: Immediate start available; apply now to join a top-tier 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. Understanding these regulations inside out will not only boost your confidence but also demonstrate your commitment to the role during any discussions.
✨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 from your previous roles where you successfully navigated regulatory challenges. This will showcase your problem-solving skills and practical knowledge during interviews.
✨Tip Number 4
Stay updated on current trends and changes in regulatory affairs by following relevant publications and joining online forums. This will help you speak knowledgeably about the industry during your interactions with us.
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 expertise.
Craft a Compelling Cover Letter: Write a cover letter that clearly outlines your motivation for applying and how your skills align with the job description. Mention your experience in new product developments and submissions in Europe and the USA.
Highlight Key Skills: In your application, emphasise your understanding of risk management within the medical device industry. This is crucial for the role and should be clearly stated in both your CV and cover letter.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any errors or typos. A polished application reflects your attention to detail, which is essential 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 expertise.
✨Showcase Relevant Experience
Prepare to discuss your previous roles and how they relate to the position. Highlight specific projects where you contributed to product submissions or compliance efforts, as this will show your practical knowledge in the field.
✨Understand Risk Management
Familiarise yourself with risk management principles within the medical device industry. Be ready to explain how you've applied these principles in past roles, as this is crucial for the role of a Regulatory Affairs Associate.
✨Ask Insightful Questions
Prepare thoughtful questions about the company's products, their regulatory strategies, and future developments. This shows your genuine interest in the role and helps you assess if the company aligns with your career goals.
