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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 hybrid or remote work options, competitive salary, and company perks.
- Why this job: Engage in varied tasks that challenge you while making a real impact in healthcare.
- Qualifications: 2+ years in a similar role with knowledge of regulatory requirements.
- Other info: Immediate start available; reach out with your CV to apply!
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. 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
Regulatory Affairs Associate (Hybrid/Remote) employer: Avd Appoint
Contact Detail:
Avd Appoint Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Regulatory Affairs Associate (Hybrid/Remote)
✨Tip Number 1
Familiarise yourself with the latest EU MDR and 510(k) requirements. Understanding 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 experts can provide you with valuable insights and potentially lead to referrals.
✨Tip Number 3
Prepare to discuss specific examples of how you've navigated regulatory challenges in your previous roles. Highlighting your problem-solving skills and adaptability will make you stand out as a candidate.
✨Tip Number 4
Research the company’s recent product launches and regulatory submissions. Being knowledgeable about their work will allow you to tailor your conversation and show genuine interest during the interview process.
We think you need these skills to ace Regulatory Affairs Associate (Hybrid/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 skills and achievements in previous roles.
Craft a Compelling Cover Letter: Write a cover letter that addresses the key requirements mentioned in the job description. Explain why you are interested in the position and how your background aligns with the company's needs, especially your experience with new product developments and submissions.
Highlight Relevant Skills: In your application, emphasise your understanding of risk management within the medical device industry. Mention any specific projects or experiences that showcase your ability to navigate regulatory requirements effectively.
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 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, especially EU MDR and 510(k) processes. Brush up on your knowledge of risk management in the medical device industry, as this will likely come up during the interview.
✨Showcase Relevant Experience
Prepare to discuss your previous roles and how they relate to the position. Highlight specific projects where you supported product developments or submissions, and be ready to explain your contributions and outcomes.
✨Ask Insightful Questions
Demonstrate your interest in the role by preparing thoughtful questions about the company's regulatory strategies and challenges. This shows that you are engaged and eager to contribute to their success.
✨Be Ready for Scenario-Based Questions
Expect to face scenario-based questions that assess your problem-solving skills in regulatory affairs. Think of examples from your past experience where you navigated complex regulatory issues and how you resolved them.
