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

Medical Device Design jobs

Sort by: -
    • 3+ years in the medical device industry in a similar Regulatory role.
    • This pivotal role involves overseeing regulatory compliance, ensuring that medical device…
    • Ensure designs meet regulatory, performance and user requirements.
    • Work within structured product development and design control processes.
    • 3+ years' medical device regulatory experience.
    • Innovative medical device SME with a strong reputation.
    • Join a leading SME where your regulatory expertise will…
    • Ensure all organisational design activity aligns with DWP design principles and the emerging Target Operating Model.
  • View similar jobs with this employer
    • The Patient Safety Monitoring Function is responsible for developing and delivering a world class vigilance system to detect and monitor safety signals for…
  • 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…
    • Improve device efficiency, stability, and manufacturability.
    • Enable affordable, scalable next-generation materials and devices.
    • Archangel engineers design and deploy low-SWaP embedded devices to enable edge AI in the air and on the ground.
    • Battery power monitoring GPS/GNSS positioning.
  • View similar jobs with this employer
    • Experience in a regulated industry, preferably within medical devices or healthcare technology.
    • Lead complaint investigations and perform root cause analysis to…
    • Improve device efficiency, stability, and manufacturability.
    • Enable affordable, scalable next-generation materials and devices.
    • As a Design Assurance Engineer, you will play a pivotal role in enabling our transition from research-focused product delivery to medical-device grade design…
    • Experience in medical device design or other highly regulated industries is desirable.
    • You will play a key role in new product introduction (NPI), working cross…
    • Moreover, it aims at establishing structure-transport-function relationships based on understanding fundamental reaction and degradation processes in both ex…
    • You have comprehensive knowledge of a recognised CAD design package, preferably with good experience of Onshape and/or Creo Parametric design software.
    • 3–5 years' experience in Product Management or Marketing within the medical device industry.
    • Medical device sales, healthcare solutions or clinical consulting…

People also searched:

interior designer
mdm
medical assistant
medical devices
medical receptionist
medical sales
medical secretary
medical writer
print
systems

Job Post Details

Senior Regulatory Professional - Medical Devices - job post

MCA Recruitment recruiting on behalf of our client
London
£55,000 - £58,000 a year - Permanent, Full-time

Job details

Pay

  • £55,000 - £58,000 a year

Job type

  • Permanent
  • Full-time

Shift and schedule

  • Monday to Friday

Location

London

Benefits

Pulled from the full job description

  • Sick pay
  • Company pension
  • Private medical insurance
  • Health & wellbeing programme
  • Company events
  • Transport links
  • On-site parking

Full job description

Job Summary

We are seeking an experienced Senior Regulatory Professional specialising in Medical Devices to join our clients dynamic team. This pivotal role involves overseeing regulatory compliance, ensuring that medical device products meet all necessary standards and regulations. The ideal candidate will possess a strong background in quality assurance and have a comprehensive understanding of medical device regulations across various markets. This position offers an excellent opportunity to contribute to innovative healthcare solutions within a collaborative and forward-thinking organisation.

Located in North London. Excellent transport links.

The hours 8.30am to 5pm, or you can do 8am to 4.30pm.Monday to Friday.

The Package

  • Salary £55,000 to £57,000 dependent on experience
  • Bonus
  • 25 days Holiday plus bank holidays
  • The company will support you with professional development, this is very important to them.
  • Private Healthcare
  • Online GP Services -Access to an online GP service

Experience

3+ years in the medical device industry in a similar Regulatory role.

  • Strong knowledge of EU MDR 2017/745, ISO 13485, and other relevant international regulatory frameworks and standards.
  • Proven ability to compile, maintain, and submit Technical Documentation, product registrations, and regulatory submissions to authorities and Notified Bodies.
  • Experienced in clinical evaluation activities, including Clinical Evaluation Plans/Reports, literature reviews, and post-market clinical follow-up.
  • Solid understanding of labelling compliance, product classification, intended use determination, and regulatory pathways during product development.
  • Skilled in post-market surveillance and vigilance activities, including adverse event reporting, PSURs, and field safety corrective actions.
  • Able to monitor, interpret and communicate regulatory changes to the business in language that is easy to understand.
  • Strong, pragmatic collaborator across Quality, Clinical, Marketing, R&D, and Operations, supporting product launches and ongoing compliance.
  • Familiarity with QMS processes and regulatory audits/Notified Body inspections, with exposure to sterile manufacturing environments considered a plus.

This role is ideal for professionals committed to advancing healthcare through rigorous regulatory oversight and quality assurance excellence.

Pay: £55,000.00-£58,000.00 per year

Benefits:

  • Company events
  • Company pension
  • Health & wellbeing programme
  • On-site parking
  • Private medical insurance
  • Sick pay

Application question(s):

  • Is your current location commutable to North London on a daily basis ?

Experience:

  • MDR 2017/745, ISO 13485 directives : 3 years (required)
  • submit Tech Docs, product regs, and regulatory submissions : 3 years (required)

Work authorisation:

  • United Kingdom (required)

Work Location: In person

Let Employers Find YouUpload Your Resume