At a Glance
- Tasks: Lead regulatory submissions for medical devices across the UK, EU, and US.
- Company: Growing medical device business with a focus on innovation.
- Benefits: Competitive salary up to £80,000 and fully remote work.
- Other info: Must be based in the UK with the right to work.
- Why this job: Take ownership in a fast-paced environment and shape regulatory strategy.
- Qualifications: 10+ years in medical device regulatory affairs and strong knowledge of EU MDR and FDA.
The predicted salary is between 80000 - 80000 € per year.
Cpl Life Sciences is partnering with a small but growing medical device business that has recently secured funding and is now looking to hire a Regulatory Submissions Lead to support its next phase of growth. This is a hands-on role with real ownership — ideal for someone who enjoys working across strategy and execution in a fast-moving environment.
You’ll be responsible for leading regulatory submissions across the UK, EU, and US, including FDA 510(k), De Novo, and Q-Subs, while acting as a key point of contact for regulators and notified bodies. Alongside submissions, you’ll play a big part in shaping regulatory strategy, ensuring compliance across the full product lifecycle, and supporting the business as it expands into new markets.
Key Responsibilities- Lead global regulatory submissions (FDA, EU MDR, UKCA)
- Prepare and manage 510(k), De Novo and FDA pre-submissions
- Represent the business in FDA and regulatory authority interactions
- Develop regulatory strategies, including classification and market pathways
- Carry out gap analysis on technical documentation and clinical evidence
- Maintain clinical evaluation reports (CERs) and technical files
- Review product claims, labelling and promotional material
- Support post-market surveillance and regulatory compliance activities
- Work closely with Quality, Clinical, R&D and commercial teams
- Around 10+ years of experience in medical device regulatory affairs
- Strong knowledge of EU MDR and FDA requirements
- Experience with 510(k), De Novo, and Q-Sub processes
- Comfortable working cross-functionally and influencing stakeholders
- Able to balance detail with a practical, commercial mindset
- Must be based in the UK and have the right to work in the UK
- Fully remote role
For more information, please reach out - This role does not offer sponsorship; you must hold the full right to work.
Regulatory Submissions Lead - Medical Devices in Liverpool employer: Cpl Life Sciences
Cpl Life Sciences is an exceptional employer, offering a dynamic and supportive work environment for the Regulatory Submissions Lead role. With a focus on employee growth and development, the company encourages innovation and collaboration, allowing you to take ownership of your projects while working remotely from anywhere in the UK. Join a small but ambitious team that values your expertise and offers the chance to make a significant impact in the medical device industry as it expands into new markets.
StudySmarter Expert Advice🤫
We think this is how you could land Regulatory Submissions Lead - Medical Devices in Liverpool
✨Tip Number 1
Network like a pro! Reach out to professionals in the medical device industry on LinkedIn or at relevant events. We can’t stress enough how valuable personal connections can be in landing that dream job.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of regulatory submissions and compliance. We recommend practising common interview questions and scenarios related to FDA and EU regulations to show you’re the right fit.
✨Tip Number 3
Showcase your hands-on experience! When discussing your background, highlight specific projects where you led regulatory submissions or developed strategies. We want to see how you’ve made an impact in previous roles.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. We’re excited to see how you can contribute to our growth in the medical device sector.
We think you need these skills to ace Regulatory Submissions Lead - Medical Devices in Liverpool
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Regulatory Submissions Lead role. Highlight your experience with FDA submissions and EU MDR compliance, as these are key for us. Use specific examples that showcase your hands-on approach and strategic thinking.
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Tell us why you’re passionate about regulatory affairs in the medical device sector. Mention how your background aligns with our needs and how you can contribute to our growth story.
Showcase Your Cross-Functional Skills:We love candidates who can work across teams! In your application, highlight any experiences where you've collaborated with Quality, Clinical, or R&D teams. This will show us you can influence stakeholders effectively.
Apply Through Our Website:Don’t forget to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it gives you a chance to explore more about our company culture and values.
How to prepare for a job interview at Cpl Life Sciences
✨Know Your Regulations
Make sure you brush up on the latest EU MDR and FDA requirements. Being able to discuss specific regulations and how they apply to the role will show that you're not just familiar with the basics, but that you’re genuinely engaged and knowledgeable about the field.
✨Showcase Your Experience
Prepare to talk about your past experiences with 510(k), De Novo, and Q-Sub processes. Have specific examples ready that highlight your hands-on experience and how you've successfully navigated regulatory submissions in the past.
✨Demonstrate Cross-Functional Collaboration
Since this role involves working closely with various teams, be ready to share examples of how you've effectively collaborated with Quality, Clinical, R&D, and commercial teams. Highlighting your ability to influence stakeholders will set you apart.
✨Ask Insightful Questions
Prepare thoughtful questions about the company’s regulatory strategy and future market expansions. This shows your interest in the role and helps you gauge if the company aligns with your career goals.
