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    • Online GP Services -Access to an online GP service.
    • 3+ years in the medical device industry in a similar Regulatory role.
    • 25 days Holiday plus bank holidays.
    • Increasing annual leave with service.
    • Drive transport network optimisation initiatives to improve service performance, fleet utilisation, route efficiency, and…
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    • Discounts on other Co-op products and services.
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    • Discounts on other Co-op products and services.
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    • 25 days holiday plus 8 days public /customary holidays & service-related holidays (pro rata).
    • Monthly pay, 33 days holiday (increasing with service), enhanced…
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    • Familiarity with specimen transport systems and laboratory workflows.
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    • These shifts may be outside of public transport operating hours.
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    • As a professional driver, you'll provide safe, reliable transport and excellent customer service across Coventry and the West Midlands.
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    • NQP Programme and Workforce Development*.
    • As a professional driver, you'll provide safe, reliable transport and excellent customer service across the West Midlands.
    • Full UK PCV Licence (Category D).
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    • Enhanced holiday entitlement with service to 33 days including bank holidays.
    • Annual loyalty payments increasing with service up to £500 each year.
    • ✅ Safe working practices and compliance with transport regulations.
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    • You would be required to work Monday to Friday driving a 16 seat PCV minibus during daylight hours on split shifts during the school term, usual hours are 7:00…

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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