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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 24000 - 32000 £ per year.
I am currently recruiting for a Regulatory Affairs Associate to work for a multi-national medical device organisation. 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.
Regulatory Affairs Consultant (Remote) employer: Avd Appoint
Contact Detail:
Avd Appoint Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Regulatory Affairs Consultant (Remote)
✨Tip Number 1
Make sure to highlight your experience with EU MDR and 510(k) submissions during any conversations. These specific regulatory frameworks are crucial for the role, and demonstrating your familiarity can set you apart from other candidates.
✨Tip Number 2
Network with professionals in the medical device industry, especially those who work in regulatory affairs. Engaging with them on platforms like LinkedIn can provide insights into the company culture and may even lead to referrals.
✨Tip Number 3
Stay updated on the latest regulatory changes and trends in the medical device sector. Being knowledgeable about current events can help you engage in meaningful discussions during interviews and show your commitment to the field.
✨Tip Number 4
Prepare to discuss specific examples of how you've managed risk in previous roles. This is a key aspect of the job, and having concrete examples ready will demonstrate your expertise and problem-solving skills.
We think you need these skills to ace Regulatory Affairs Consultant (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 supporting new product developments and compliance with regulatory requirements.
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 sure it stands out.
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 Relevant Experience
Highlight your previous experience in regulatory affairs, particularly any specific projects or submissions you've worked on. Be ready to provide examples that demonstrate your knowledge and skills in this area.
✨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 roles and how they relate to regulatory compliance.
✨Ask Insightful Questions
Prepare thoughtful questions about the company's products, their regulatory strategies, and the team dynamics. This shows your genuine interest in the role and helps you assess if the company is the right fit for you.
