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    • 3+ years' medical device regulatory experience.
    • Innovative medical device SME with a strong reputation.
    • Key role supporting EU MDR compliance and product growth…
  • View similar jobs with this employer
    • This role focuses on advising clients on the regulatory, Quality and compliance aspects of medical devices, through a strong understanding of regulatory and…
    • A basic knowledge of medical terminology is needed, as well as knowledge of a scientific investigative methodologies and clinical research methodologies.
    • Operating as part of a high-performing regional team, you will act as a critical bridge between commercial sponsors and the NHS.
    • Experience with Class II or III medical product development is preferred.
    • Relevant experience of working within medical device (or equivalent) organisation with…
    • Partner with product management and R&D to align on product strategy/roadmap.
    • Vitalograph is the world’s leading manufacturer of medical respiratory diagnostic…
    • Strong knowledge of orthopaedic or medical device engineering.
    • The ideal candidate will be from a technical background, preferable with a few years of…
    • Acting as the UK Quality representative for medical device sales, service, and distribution activities.
    • Minimum of 3 years’ experience in ISO9001 Quality…
    • Partner with product management and R&D to align on product strategy/roadmap.
    • Vitalograph is the world’s leading manufacturer of medical respiratory diagnostic…
    • Exposure to IoT device product development processes.
    • Product Managers for each product.
    • Experience working with firmware, embedded systems or IoT products.
    • O Company-contributed medical insurance.
    • O 23 days annual leave.
    • O Company-contributed pension scheme.
    • O 4x salary death-in-service benefit.
    • Learning the scientific and commercial aspects of advanced preclinical products and services.
    • They are seeking a scientifically minded individual looking to…
    • Supporting the development of connected product, IoT and digital service strategies.
    • Understanding of how connected products and digital services create…
    • Access to our flexible benefits from private medical insurance to dental cover.
    • Apply now for the position of Design Change Lead, and you will lead end-to-end…
    • Proven leader of complex, cross‑functional programmes within manufacturing or engineered product environments.

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Job Post Details

BMS Performance Ltd logo

Regulatory Medical Affairs - job post

BMS Performance Ltd
4.5 out of 5 stars
North West London
£50,000 - £56,000 a year - Permanent, Full-time

Job details

Pay

  • £50,000 - £56,000 a year

Job type

  • Permanent
  • Full-time

Location

North West London

Full job description

Join a leading SME where your regulatory expertise will directly impact advanced wound care products that improve patient outcomes.

Senior Regulatory Affairs Specialist | Advanced Wound Care & Infection Prevention

NW London (office based 5 days per week)
£56K + Bonus + Excellent Benefits
Strong knowledge of EU MDR 2017/745 & ISO 13485 required

Looking for a regulatory role where your work directly supports products that improve patient outcomes?
Learning and development supported - clear progression!

The company is a well-regarded SME and a leading force in advanced wound care and infection prevention, with a product portfolio backed by strong clinical evidence.

Why This Role?

  • Senior RA position with real ownership and influence
  • Innovative medical device SME with a strong reputation
  • Key role supporting EU MDR compliance and product growth
  • Diverse, clinically meaningful wound care portfolio
  • Clear progression and ongoing development opportunities

What You'll Do:

  • Lead and maintain EU MDR technical documentation
  • Support Class I to Class II product transitions
  • Collaborate with Clinical, R&D, Marketing and Operations teams
  • Manage regulatory submissions and compliance activities
  • Engage with Notified Bodies and Competent Authorities
  • Help shape global regulatory strategy

Requirements:

  • 3+ years' medical device regulatory experience
  • Strong knowledge of EU MDR 2017/745 & ISO 13485
  • Experienced with technical documentation
  • Detail-focused, proactive and commercially aware
  • Excellent stakeholder management skills

Benefits:

  • £52-56K basic
  • 5% annual bonus
  • 25 days holiday + bank holidays

Ready to take ownership of a high-impact regulatory portfolio? Apply now.

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