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For Companies At a Glance
- Tasks: Manage regulatory submissions and ensure compliance in the medical device industry.
- Company: Cutting-edge medical device manufacturer with a real-world impact.
- Benefits: Competitive salary, 4-day working week, and permanent position.
- Why this job: Join a dynamic team and shape the future of healthcare technology.
- Qualifications: Experience with medical device regulations and strong QMS knowledge.
- Other info: Flexible work-life balance and opportunities for professional growth.
The predicted salary is between 36000 - 60000 £ per year.
A 4 day working week, allowing for more flexibility and better work life balance.
About Our Client
Our client is a cutting edge medical device manufacturer. They have multiple marketed products, as well as new products awaiting registration in UK, EU and ROW markets.
Job Description
- Coordinate and manage regulatory submissions and approvals in line with industry standards.
- Ensure compliance with applicable regulations and guidelines within the life sciences industry.
- Monitor regulatory changes and update internal processes as required.
- Provide strategic advice on regulatory matters to support business objectives.
- Develop and maintain relationships with regulatory authorities and key stakeholders.
- Prepare and review documentation to ensure accuracy and compliance.
- Collaborate with internal teams to align regulatory strategies with organisational goals.
- Support audits and inspections related to regulatory compliance.
The Successful Applicant
- Proven record of working with Medical device regulations, and liaising with regulatory bodies.
- Good knowledge of QMS activities.
What's on Offer
- Competitive salary
- 4 Day Working week
- Permanent position based in West London
Regulatory Affairs Manager (Medical Devices) in London employer: Michael Page (UK)
Contact Detail:
Michael Page (UK) Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Regulatory Affairs Manager (Medical Devices) in London
✨Tip Number 1
Network like a pro! Reach out to professionals in the regulatory affairs field on LinkedIn or at industry events. Building connections can lead to job opportunities that aren't even advertised yet.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of medical device regulations. We recommend creating a cheat sheet of key regulations and compliance standards to discuss confidently during your interview.
✨Tip Number 3
Showcase your experience with regulatory submissions and approvals. Use specific examples from your past roles to demonstrate how you’ve successfully navigated the regulatory landscape, making sure to highlight any relationships you've built with regulatory authorities.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive about their job search!
We think you need these skills to ace Regulatory Affairs Manager (Medical Devices) in London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Regulatory Affairs Manager role. Highlight your experience with medical device regulations and any relevant QMS activities. We want to see how your background aligns with our cutting-edge business!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about regulatory affairs in the medical device sector. Share specific examples of how you've navigated regulatory submissions and compliance in the past.
Showcase Your Communication Skills: In this role, you'll need to liaise with regulatory bodies and internal teams. Make sure your application reflects your strong communication skills. We love candidates who can clearly articulate complex regulatory matters!
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you don’t miss out on any important updates. Plus, we love seeing applications come through our own platform!
How to prepare for a job interview at Michael Page (UK)
✨Know Your Regulations
Make sure you brush up on the latest medical device regulations and guidelines. Familiarise yourself with the specific requirements for the UK, EU, and ROW markets. This will show your potential employer that you're not just knowledgeable but also proactive about staying updated.
✨Showcase Your Experience
Prepare to discuss your previous experience in regulatory affairs, especially any direct interactions with regulatory bodies. Use specific examples to illustrate how you've successfully managed submissions and ensured compliance in past roles.
✨Understand Their Business
Research the company’s marketed products and any new ones they have in the pipeline. Understanding their business model and how regulatory affairs fit into their strategy will help you align your answers with their objectives during the interview.
✨Prepare Questions
Have a few thoughtful questions ready to ask at the end of the interview. This could be about their approach to regulatory changes or how they collaborate with internal teams. It shows your interest in the role and helps you gauge if the company is the right fit for you.
