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Senior Regulatory Specialist

CAPU Search

United Kingdom

Remote

GBP 80,000 - 100,000

3 days ago
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Job summary

An exciting opportunity awaits with a forward-thinking neuromodulation company seeking a Senior Regulatory Specialist. In this fully remote role, you will take charge of rewriting procedures and supporting critical MDR transition efforts. With a focus on collaboration and problem-solving, you will thrive in a dynamic environment where your expertise will directly impact the compliance landscape of medical devices. Join a mission-driven team dedicated to improving lives through innovative technology, and enjoy the flexibility of remote work while making a real difference in the industry.

Benefits

Flexible working

Remote work opportunity

Impactful work in a mission-driven team

Qualifications

  • 5–8 years' experience in regulatory affairs at the Senior Specialist level.
  • Strong people skills for collaborative and persuasive interactions.

Responsibilities

  • Rewrite procedures and support MDR transition efforts.
  • Maintain compliance and manage regulatory activities for medical devices.

Skills

Regulatory Affairs

People Skills

Problem Solving

EU MDR Compliance

Job description

Senior Regulatory Specialist – Fully Remote Opportunity

We're currently working on an exciting fully remote Senior Regulatory Specialist role with a UK-based neuromodulation company.

The Role: This is more than just maintaining compliance; you’ll be rewriting procedures, cutting red tape, and supporting MDR transition efforts (currently at the technical file review stage). You’ll report directly to the Head of Regulatory and act as their right hand on a business-critical project.

What They’re Looking For:

  • 5–8 years' experience in regulatory affairs, ideally at the Senior Specialist level.
  • Someone who's confident being dropped into the deep end and thrives in a hands-on, solution-focused environment.
  • Strong people skills—there’ll be pushback and politics, so you’ll need a collaborative, persuasive style.
  • Experience with EU MDR, rewriting regulatory SOPs, and managing compliance activities for medical devices.

Why This Role?

  • 100% remote, with flexible working.
  • A chance to make a real impact and cut through bureaucracy.
  • Be part of a mission-driven team improving lives through advanced neuromodulation technology.
Seniority level

Mid-Senior level

Employment type

Full-time

Job function

Other

Industries

Medical Equipment Manufacturing

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