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Medical Biochemistry jobs in London

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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…
    • Full-time/permanent - 37.5 hours per week.
    • Salary - £30,000 - £35,000 per annum (depending on experience) + excellent benefits.
    • Bioanalyst: - LC-MS/MS - 3-month fixed term contract (with the possibility to extend or become permanent).
    • Hours: 37.5 per week (onsite, across 5 days Monday-…
    • Eramol (UK) Ltd is a privately-owned organisation based in Sevenoaks, Kent providing manufacturing and distribution services for clinical trials.
    • Leads the medical safety contributions of global regulatory submissions for new products, formulations or indications.
    • Minimum 2-5 years of Clinical Development, Medical Affairs or Drug Safety/Pharmacovigilance experience; other relevant medical affairs experience may be…
    • Biochemistry with focus on immunology.
    • Important： Please read before your application*.
    • To those interested in this position, the position office will based…
    • Perform review of medical/scientific literature to identify literature relevant for signal detection activities and aggregate reporting for assigned products,…
    • Salary:* £22.00 -£31.00ph.
    • Hours:* 37.5 hours per week.
    • Contract Type:* Temporary / Full-Time.
    • We are currently seeking an experienced and motivated *Band 6…
    • Educational Background: BSc (or equivalent) in a life sciences field, featuring solid knowledge of general biochemistry, cell biology, and molecular biology.
    • Monitors the medical literature for additional sources of product information and content for use in the creation of medical information materials.
    • Science Technician - Full-Time (5 Days per Week) | Lambeth.
    • Are you an experienced Science Technician looking for your next opportunity in a thriving school…
    • Potential to develop specialist expertise in medical device regulations.
    • Ensuring product compliance with ISO 13485, IEC 62304 and relevant medical device…
    • Job Title:* Lead Biomedical Scientist.
    • Pay Rates:* £27.94 (TBC).
    • Shift Patterns*: 37.5 hours per week.
    • The Deputy Head of Pathology, Phlebotomy and Point of…
    • Hours:* 37.5 hours per week.
    • Salary: £20-£26phdepending on shift pattern.
    • We are currently seeking an experienced HCPC Registered Biomedical Scientist* to…

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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