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Medical Device Engineer jobs in England

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    • 3+ years in the medical device industry in a similar Regulatory role.
    • This pivotal role involves overseeing regulatory compliance, ensuring that medical device…
    • Dynamic (hybrid) working: Where project needs allow, we will seek to accommodate a blended approach to on-site and remote working such as being onsite when…
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    • Enthusiasm to help build the careers of our less experienced engineers.
    • We are looking for a Consumer Electronics Engineer with experience in bringing high-…
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    • This role focuses on advising clients on the regulatory, Quality and compliance aspects of medical devices, through a strong understanding of regulatory and…
    • Company : Safran Electrical & Power Job field : Testing Location : Sl1 4ry , England , United Kingdom Contract type : Permanent Contract duration : Full-time…
    • We are currently looking for a Field Service Engineer for the London area of the UK, who will have the possibility to conducts service, repair and/or…
    • Knowledge of regulatory requirements for Class I medical devices to MDD and MDR.
    • You’ll be a technically capable and detail orientated engineer with experience…
    • This full-time, on-site role offers the opportunity to work on innovative hardware used in diverse sectors such as healthcare, retail, and events.
    • Commissioning and Testing: Lead the commissioning process of electrical protection systems, including relays, switchgear, generators, transformers, and other…
    • Device physics background (e.g organic and inorganic FETs/ECTs etc).
    • Innovation and implementation transduction mechanisms for biosensors, with the focus on…
    • Minimum of 2-3 years in a highly technical manufacturing environment.
    • Ability to conduct equipment qualifications, software, and process validation, including…
    • 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…
    • The ideal candidate will have a minimum 3 years experience in software design & PLC software experience (Rockwell / Allen Bradley) and would have previously…
    • The company specialises in the design, engineering and manufacture of advanced test interfaces and electronic solutions that support the development, validation…
    • Experience with Electromagnets, complex assemblies and medical devices.
    • Competitive Salary Up to £42,000 depending on experience.

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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

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