Skip to main content
Post your CV and find your next job on Indeed!

Medical Affairs Manager jobs

Sort by: -
    • 3+ years' medical device regulatory experience.
    • Innovative medical device SME with a strong reputation.
    • Join a leading SME where your regulatory expertise will…
    • Flexible working, Full-time, Job share, Part-time.
    • The post holder will manage specific aspects of the research support function, work on specific projects and…
    • It will do this by bringing together a fusion of our capabilities across both medicines and medical devices to enable licensing and market access, as well as…
    • Supporting client delivery: contributing to strategic planning and consultancy services.
    • Team contribution and development: supporting project teams and…
    • Interpersonal skills: you will act as the client relationship manager for individual clients and account manage issues for existing and new clients within a…
    • Ensure company’s regulatory affairs activities are conducted according to relevant regulations,laws, and standards.
    • At least 3 years of experience as a consortium manager or regulatory affairs consultant working with international chemical regulations, especially REACH.
  • View similar jobs with this employer
    • Experienced field medical professional with 3+ years in an MSL role - Bringing proven success in engaging healthcare professionals and translating scientific…
    • Strategic ICS-level role with high autonomy*.
    • Innovative MedSurg & wound care portfolio*.
    • Working at ICS level, you'll engage senior NHS stakeholders, shape…
    • Up to £26.04 phr PAYE, or £34.09 phr Umbrella.
    • Manage the preparation and delivery of regulatory submissions to Health Authorities across regional and national…
    • Proven experience working in a regulatory affairs or highly regulated environment.
    • Our Client is seeking a highly organised and detail‑oriented Regulatory…
  • View similar jobs with this employer
    • New entrants to the Civil Service will start their role on the salary band minimum of £60,778.
    • This is a full-time opportunity, on a permanent basis.
    • Within this, we are looking to grow our healthcare and life science practice with highly motivated and collaborative individuals who will bring an understanding…
    • Supporting client delivery: contributing to strategic planning and consultancy services.
    • Team contribution and development: supporting project teams and…
    • Engagements will involve working with clients to resolve their most pressing challenges in franchise/portfolio/disease strategy and asset positioning; business…

People also searched:

operations manager
retail manager
store manager
supervisor
team leader
medical assistant
medical devices
medical receptionist
medical sales
medical secretary

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.

Let Employers Find YouUpload Your Resume