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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
Familiarise yourself with the latest EU MDR and 510(k) requirements. Being well-versed in these regulations will not only boost your confidence during interviews but also demonstrate your commitment to staying updated in the field.
✨Tip Number 2
Network with professionals in the regulatory affairs sector, especially those who have experience in medical devices. Engaging with industry groups on platforms like LinkedIn can provide valuable insights and potentially lead to referrals.
✨Tip Number 3
Prepare to discuss specific examples from your previous roles that highlight your experience with product submissions and compliance. Real-life scenarios can effectively showcase your problem-solving skills and understanding of risk management.
✨Tip Number 4
Research the company’s recent projects and initiatives in the medical device space. Showing that you are informed about their work can set you apart and demonstrate your genuine interest in joining their team.
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 not only outlines your qualifications but also expresses your enthusiasm for the role. Mention why you are interested in working for a multi-national medical device organisation and how you can contribute to their success.
Highlight Relevant Skills: In your application, emphasise your understanding of risk management within the medical device industry. This is crucial for the role, so make sure to provide concrete examples of how you've applied this knowledge in previous positions.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any spelling or grammatical errors. 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 ready to discuss how they impact product submissions.
✨Showcase Your Experience
Prepare specific examples from your previous roles that demonstrate your experience in regulatory affairs. Highlight any successful submissions you've managed 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 past 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.
