Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- Tasks: Manage global regulatory approvals for medical devices and support documentation.
- Company: Join a leading engineering firm known for innovation and international reach.
- Benefits: Enjoy a competitive salary, hybrid work options, and growth opportunities.
- Why this job: Be part of a dynamic team with ambitious growth plans and a focus on stability.
- Qualifications: 2+ years in Regulatory Affairs, experience with medical devices, and post-market surveillance.
- Other info: Immediate start available; apply now to secure your future!
The predicted salary is between 24000 - 40000 £ per year.
I am currently recruiting for a Regulatory Affairs Associate to work for a leading engineering organisation based in Cheshire, but on a hybrid basis. Salary up to £40,000 + Benefits.
The company are leaders within their field of expertise and are seen as the go-to organisation within their specialist product area, not only in the UK, but on an international basis. They have multiple offices throughout the UK, as well as being strategically positioned throughout the world. They have gone from strength to strength over recent years and via organic growth as well as a range of acquisitions they have strengthened their client offering ensuring they stay at the forefront of the market.
To support the growth of the business they now have the need to appoint a Regulatory Affairs Associate on a permanent basis. In this role as a Regulatory Affairs Associate, you will be responsible for the regulatory approvals on a global basis for a range of medical devices. This will include the necessary documentation to support with the approvals process. You will also be involved in post market surveillance, vigilance reporting, field safety corrective actions (recalls) and risk management.
Essential Requirements:
- At least 2 years' experience as a Regulatory Affairs Associate or similar
- Experience with Post Market Surveillance
- Experience with vigilance reporting
- Experience with Field Safety corrective action (recalls)
- Previous experience with medical devices (ideally class II and class III)
Desirable Requirements:
- Risk management
This is a fantastic opportunity for a Regulatory Affairs Associate to work for a leader within their field. The company has very ambitious, but realistic growth plans and this role is part of the business's succession planning, so stability and progression are both on offer with this opportunity.
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. Either apply direct or contact Adam on 01183 366 100.
Regulatory Affairs Associate employer: AVD Appoint Ltd
Contact Detail:
AVD Appoint Ltd Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Regulatory Affairs Associate
✨Tip Number 1
Familiarise yourself with the specific regulations and guidelines related to medical devices, especially Class II and III. This knowledge will not only help you in interviews but also demonstrate your commitment to the role.
✨Tip Number 2
Network with professionals in the regulatory affairs field, particularly those who have experience with medical devices. Engaging with industry groups or attending relevant webinars can provide valuable insights and connections that may lead to job opportunities.
✨Tip Number 3
Prepare to discuss your experience with post-market surveillance and vigilance reporting in detail. Be ready to share specific examples of how you've handled these processes in previous roles, as this will be crucial for the position.
✨Tip Number 4
Research the company’s recent projects and acquisitions to understand their growth strategy. Being knowledgeable about their operations will allow you to tailor your conversation during interviews and show that you're genuinely interested in contributing to their success.
We think you need these skills to ace Regulatory Affairs Associate
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your relevant experience in regulatory affairs, particularly with medical devices. Emphasise your skills in post market surveillance and vigilance reporting, as these are essential for the role.
Craft a Compelling Cover Letter: Write a cover letter that specifically addresses the job description. Mention your experience with class II and class III medical devices, and explain how your background aligns with the company's growth plans.
Highlight Key Achievements: In both your CV and cover letter, include specific examples of your achievements in previous roles. This could be successful regulatory approvals you’ve managed or improvements you’ve made in risk management processes.
Proofread Your Application: Before submitting, carefully proofread your application 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 Ltd
✨Know Your Regulations
Familiarise yourself with the key regulations and guidelines relevant to medical devices, especially those pertaining to class II and class III products. Being able to discuss these confidently will show your expertise and readiness for the role.
✨Prepare for Scenario Questions
Expect questions that ask you to describe how you've handled post-market surveillance or vigilance reporting in the past. Prepare specific examples that highlight your problem-solving skills and attention to detail.
✨Showcase Your Communication Skills
As a Regulatory Affairs Associate, you'll need to communicate complex regulatory information clearly. Be prepared to demonstrate your ability to convey technical details effectively, both verbally and in writing.
✨Research the Company
Understand the company's position in the market and their recent growth strategies. This knowledge will help you tailor your answers and show your genuine interest in being part of their ambitious plans.
