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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 a real 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. Attend webinars or join relevant LinkedIn groups to connect with others who can provide insights or even referrals for opportunities at companies like us.
✨Tip Number 3
Prepare to discuss specific examples of how you've navigated regulatory challenges in past roles. Being able to articulate your experience with risk management and compliance will set you apart from other candidates.
✨Tip Number 4
Stay updated on industry trends and changes in regulations. Showing that you're proactive about your professional development can impress hiring managers and indicate that you're ready to contribute from day one.
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 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 show that you are well-prepared for the challenges of the position.
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 recent changes and be ready to discuss how they impact product submissions.
✨Showcase Your Experience
Prepare specific examples from your past roles that demonstrate your experience in regulatory affairs. Highlight any successful submissions you've been involved with and the outcomes of those projects.
✨Understand Risk Management
Be prepared to talk about risk management in the context of medical devices. Discuss how you have identified and mitigated risks in previous projects, as this is crucial for the role.
✨Ask Insightful Questions
Prepare thoughtful questions about the company's products, their regulatory strategy, and the team dynamics. This shows your genuine interest in the role and helps you assess if it's the right fit for you.
