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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 remote work options, competitive salary, bonuses, and additional 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; send your CV ASAP to seize this opportunity!
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.
Locations
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 online forums or LinkedIn groups where you can engage with others, share insights, and learn about industry trends that could give you an edge.
✨Tip Number 3
Prepare for potential interviews by practising common regulatory scenarios. Think about how you would handle specific compliance challenges or product submissions, as this will showcase your problem-solving skills.
✨Tip Number 4
Stay updated on recent changes in medical device regulations. Subscribe to industry newsletters or follow regulatory bodies on social media to ensure you're aware of any new developments that could impact your work.
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 clearly outlines your motivation for applying and how your background aligns with the role. Mention your experience with new product developments and submissions in both 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, so make it stand out in your documents.
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 recent changes and be prepared to discuss how they impact product submissions.
✨Showcase Your Experience
Be ready to share specific examples from your previous roles that demonstrate your experience in regulatory affairs. Highlight any successful submissions you've been involved with and the outcomes.
✨Understand Risk Management
Familiarise yourself with risk management principles within 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 products, regulatory challenges, and team dynamics. This shows your genuine interest in the role and helps you assess if the company is the right fit for you.
