Senior Regulatory Affairs Leader – MedTech (EMEA)
Senior Regulatory Affairs Leader – MedTech (EMEA)

Senior Regulatory Affairs Leader – MedTech (EMEA)

Full-Time 48000 - 72000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Lead regulatory affairs projects and ensure compliance for innovative medical devices.
  • Company: Top MedTech recruitment agency in the UK with a focus on innovation.
  • Benefits: Competitive salary, flexible working options, and opportunities for professional growth.
  • Why this job: Make a real difference in healthcare by shaping the future of medical technology.
  • Qualifications: Experience in project management and knowledge of European regulatory frameworks required.
  • Other info: Join a dynamic team dedicated to advancing medical solutions across EMEA.

The predicted salary is between 48000 - 72000 £ per year.

A leading MedTech recruitment agency in the United Kingdom is seeking a Senior Regulatory Affairs Consultant to lead RA/QA workstreams for a major Medical Device organization.

Key responsibilities include:

  • Managing compliance
  • Overseeing regional OEM work
  • Facilitating change notifications

The ideal candidate will have:

  • Proven project management experience
  • Deep knowledge of European regulatory frameworks
  • Familiarity with ERP systems

This high-impact consultancy role offers an opportunity to contribute to innovative medical solutions.

Senior Regulatory Affairs Leader – MedTech (EMEA) employer: elemed

As a leading MedTech recruitment agency, we pride ourselves on fostering a dynamic and inclusive work culture that prioritises employee growth and innovation. Our team enjoys competitive benefits, ongoing professional development opportunities, and the chance to make a meaningful impact in the medical device sector, all while working in the vibrant environment of the United Kingdom.
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Contact Detail:

elemed Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Senior Regulatory Affairs Leader – MedTech (EMEA)

Tip Number 1

Network like a pro! Reach out to industry professionals on LinkedIn or attend MedTech events. We can’t stress enough how personal connections can open doors for you.

Tip Number 2

Prepare for interviews by brushing up on your knowledge of European regulatory frameworks. We recommend practising common interview questions and scenarios related to compliance and project management.

Tip Number 3

Showcase your project management skills! Be ready to discuss specific examples where you’ve successfully led RA/QA workstreams. We want to see how you can contribute to innovative medical solutions.

Tip Number 4

Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. We’re here to help you land that Senior Regulatory Affairs role!

We think you need these skills to ace Senior Regulatory Affairs Leader – MedTech (EMEA)

Regulatory Affairs
Quality Assurance (QA)
Project Management
European Regulatory Frameworks
Compliance Management
Change Notification Facilitation
OEM Work Oversight
ERP Systems Familiarity
Analytical Skills
Communication Skills
Problem-Solving Skills
Attention to Detail
Leadership Skills

Some tips for your application 🫡

Tailor Your CV: Make sure your CV is tailored to highlight your experience in regulatory affairs and project management. We want to see how your skills align with the key responsibilities mentioned in the job description.

Showcase Your Knowledge: Demonstrate your deep understanding of European regulatory frameworks in your application. We’re looking for candidates who can navigate these regulations with ease, so don’t hold back on sharing relevant examples.

Be Clear and Concise: When writing your cover letter, keep it clear and concise. We appreciate straightforward communication, so get to the point while still showcasing your passion for the role and the MedTech industry.

Apply Through Our Website: We encourage you to apply through our website for a smoother application process. It helps us keep track of your application and ensures you don’t miss out on any important updates from us!

How to prepare for a job interview at elemed

Know Your Regulations

Make sure you brush up on the latest European regulatory frameworks relevant to MedTech. Being able to discuss specific regulations and how they impact compliance will show that you're not just familiar with the basics, but that you’re ready to lead.

Showcase Project Management Skills

Prepare examples of your past project management experiences, especially those related to RA/QA workstreams. Use the STAR method (Situation, Task, Action, Result) to structure your answers and highlight your ability to manage complex projects effectively.

Familiarise Yourself with ERP Systems

Since familiarity with ERP systems is a key requirement, take some time to review the systems you've used in the past. Be ready to discuss how you’ve leveraged these tools to enhance compliance and streamline processes in your previous roles.

Prepare for Change Management Questions

Given the role involves facilitating change notifications, think about times when you've successfully managed change within an organisation. Be prepared to discuss your approach to overcoming resistance and ensuring smooth transitions.

Senior Regulatory Affairs Leader – MedTech (EMEA)
elemed
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  • Senior Regulatory Affairs Leader – MedTech (EMEA)

    Full-Time
    48000 - 72000 £ / year (est.)
  • E

    elemed

    50-100
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