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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 with a strong reputation.
- Benefits: Enjoy remote work options, competitive salary, bonuses, and company perks.
- Why this job: Engage in varied tasks that challenge you while making an impact in healthcare.
- Qualifications: 2+ years in regulatory affairs with knowledge of EU MDR & 510(k) requirements.
- Other info: Immediate start available; send your CV ASAP!
The predicted salary is between 30000 - 40000 £ 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.
Medical Devices Regulatory Analyst (Remote) employer: Avd Appoint
Contact Detail:
Avd Appoint Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Medical Devices Regulatory Analyst (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 medical device regulatory field. Join relevant LinkedIn groups or attend webinars to connect with others who can provide insights and potentially refer you to opportunities at companies like us.
✨Tip Number 3
Prepare for potential interviews by practising common regulatory affairs scenarios. Be ready to discuss how you've handled compliance challenges in the past, as this will showcase your problem-solving skills and experience.
✨Tip Number 4
Stay updated on industry trends and changes in regulations. Subscribing to relevant newsletters or following key organisations will help you stay informed, making you a more attractive candidate for the role.
We think you need these skills to ace Medical Devices Regulatory Analyst (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 showcases your passion for the medical device industry and your understanding of regulatory requirements. Mention how your previous experience aligns with the responsibilities of the role.
Highlight Key Skills: In your application, emphasise your working knowledge of regulatory requirements and risk management within the medical device sector. This will help you stand out as a candidate who meets the essential 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 EU MDR and 510(k) requirements. Brush up on the latest updates and be prepared to discuss how these regulations impact product development.
✨Showcase Your Experience
Be ready to share specific examples from your previous roles that demonstrate your knowledge of regulatory affairs. Highlight any successful submissions you've worked on and the outcomes.
✨Understand Risk Management
Familiarise yourself with risk management processes in the medical device industry. Be prepared to discuss how you have applied these principles in your past work and their importance in regulatory compliance.
✨Ask Insightful Questions
Prepare thoughtful questions about the company's regulatory strategies and challenges they face in the market. This shows your genuine interest in the role and helps you assess if it's the right fit for you.
