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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 difference.
- Benefits: Enjoy hybrid or remote work, competitive salary, and company perks.
- Why this job: Engage in varied tasks within a dynamic environment that challenges you.
- Qualifications: 2+ years in a similar role with knowledge of regulatory requirements.
- Other info: Immediate start available; apply now with your CV!
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 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
Stay updated on current trends and changes in regulatory affairs by following relevant publications and joining online forums. This knowledge can help you stand out as a candidate who is proactive and well-informed.
✨Tip Number 4
Prepare for potential interview questions by practising how you would handle specific regulatory scenarios. Being able to articulate your thought process and problem-solving skills will impress hiring managers.
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 any work related to EU MDR and 510(k) submissions. Use specific examples to demonstrate your knowledge of regulatory requirements.
Craft a Compelling Cover Letter: Write a cover letter that not only outlines your qualifications but also expresses your enthusiasm for the role. Mention your understanding of risk management in the medical device industry and how it aligns with the company's goals.
Highlight Relevant Experience: In your application, emphasise your 2+ years of experience in a similar position. Detail any specific projects or achievements that showcase your ability to support new product developments and compliance with regulatory requirements.
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 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 expertise.
✨Showcase Relevant Experience
Prepare to discuss your previous roles in regulatory affairs, particularly any specific projects where you contributed to product submissions. Highlight your experience with risk management and how it applies to the medical device industry.
✨Ask Insightful Questions
Prepare thoughtful questions about the company's products, their regulatory strategies, and the challenges they face in compliance. This shows your genuine interest in the role and helps you assess if the company is the right fit for you.
✨Demonstrate Adaptability
Since the role involves hybrid or remote work, be ready to discuss how you manage your time and stay organised in a flexible work environment. Share examples of how you've successfully adapted to changing circumstances in past positions.
