Hybrid Regulatory Lead: EU MDR and FDA QSMR Strategy in Crewe

Hybrid Regulatory Lead: EU MDR and FDA QSMR Strategy in Crewe

Crewe Full-Time 50000 - 55000 £ / year (est.) No working from home possible
Network Scientific Recruitment

At a Glance

  • Tasks: Lead regulatory strategies and manage EU MDR and US submissions for innovative med-tech products.
  • Company: Global med-tech company with a focus on regulatory excellence.
  • Benefits: Competitive salary, performance bonus, and hybrid working options.
  • Other info: Join a high-impact team with opportunities for professional growth.
  • Why this job: Make a real impact in a dynamic environment while shaping the future of healthcare.
  • Qualifications: Experience in regulatory affairs and strong strategic management skills.

The predicted salary is between 50000 - 55000 £ per year.

Network Scientific Recruitment seeks an experienced Senior Regulatory Affairs Specialist for a global med-tech company with Crewe offices.

You will define and lead regulatory strategies, manage EU MDR and US 510(k)/QSMR submissions, and align with market access plans.

The role is permanent, full-time and hybrid, offering £50,000–£55,000 with a performance bonus.

You will work in a dynamic, high-impact environment and support regulatory excellence across geographies.

#J-18808-Ljbffr

Hybrid Regulatory Lead: EU MDR and FDA QSMR Strategy in Crewe employer: Network Scientific Recruitment

Network Scientific is an excellent employer for those looking to kickstart their career in the environmental testing sector. Located in Didcot, Oxfordshire, we offer a supportive work culture that prioritises employee growth through comprehensive training and hands-on experience in analytical techniques. Our commitment to ethical practices and candidate care ensures that you will be part of a team that values your contributions and fosters a rewarding work environment.

Network Scientific Recruitment

Contact Details:

Network Scientific Recruitment Recruitment Team

We think you need these skills to ace Hybrid Regulatory Lead: EU MDR and FDA QSMR Strategy in Crewe

Regulatory Strategy Development
EU MDR Knowledge
US 510(k) Submission Experience
QSMR Expertise
Market Access Alignment
Regulatory Affairs
Project Management