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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…
    • Uniphar Medtech comprises 10 businesses across 21 markets and is the medical device arm of the Uniphar Group.
    • Provide Clinical Support to Customers in the area…
    • Managing and growing strategic accounts across the territory.
    • Demonstrated success in territory management and account development.
    • Reviewing sales results and using territory insight to guide activity.
    • Managing and developing your territory in line with wider business goals.
    • Strong commission structure with uncapped earning potential (OTE £24K+).
    • Clear progression pathways supported by structured training and internal promotion.
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    • You will be seeking opportunities to upsell, cross sell and maximise the business presence within their neurosurgery portfolio of devices, capital equipment and…
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    • As a Territory Manager, you’ll nurture existing relationships and forge new partnerships across Primary and Secondary Care.
    • £48,000 base + OTE £8,000£10,000 (uncapped) Full-time Hybrid.
    • You'll lead clinical and operational teams, manage performance, and be the person your NHS…
  • View similar jobs with this employer
    • As a Territory Manager, you’ll nurture existing relationships and forge new partnerships across Primary and Secondary Care.
  • View similar jobs with this employer
    • As a Territory Manager, you’ll nurture existing relationships and forge new partnerships across Primary and Secondary Care.
  • View similar jobs with this employer
    • As a Territory Manager, you’ll nurture existing relationships and forge new partnerships across Primary and Secondary Care.
    • Vitalograph is the world’s leading manufacturer of medical respiratory diagnostic devices and software, used in the diagnosis of respiratory disorders, and…
    • Vitalograph is the world’s leading manufacturer of medical respiratory diagnostic devices and software, used in the diagnosis of respiratory disorders, and…
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    • Experience in a medical device sales role with a successful track record.
    • Having excellent standards in territory / journey and business preparation and…
  • View similar jobs with this employer
    • Experience in a medical device sales role with a successful track record.
    • Having excellent standards in territory / journey and business preparation and…

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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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