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Biomedical Engineer jobs in England

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    • This is a full time, on-site position based in Sheffield.
    • This is an established healthcare manufacturer operating within a regulated medical device environment…
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    • This role offers technical influence, visibility, and the chance to shape how systems engineering is applied across the magnet lifecycle.
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    • For ongoing projects nationwide, Medi-Plumb Installations (MPI) are looking for Medical, Laboratory, and Industrial Gas Engineers.
    • Minimum of 2-3 years in a highly technical manufacturing environment.
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    • Degree or HNC/HND in Engineering beneficial (ideally mechanical or biomedical).
    • We’re looking for a proactive QA Quality Engineer to support our Quality…
    • This role is central to ensuring our ventilation products meet the highest standards of performance, reliability, and regulatory compliance.
    • The ideal candidate will have experience in innovative research, leading to product development, particularly in the development of highly sensitive (bio)…
    • Competitive Salary Up to £42,000 depending on experience.
    • 6.6 working weeks paid holiday per year including Summer and Christmas / New Year closures.
    • Salary:* £50,000 - £60,000 OTE (Inc Commission) + Excellent Benefits.
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Job Post Details

Technical Documentation and Development Engineer - job post

Michael Page
3.7 out of 5 stars
Sheffield
£42,000 a year - Permanent
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Job details

Pay

  • £42,000 a year

Job type

  • Permanent

Location

Sheffield

Full job description

  • The salary for this role is £42k.
  • This is a full time, on-site position based in Sheffield.

About Our Client

This is an established healthcare manufacturer operating within a regulated medical device environment, focused on improving patient outcomes through product innovation and continuous improvement. The business has a growing portfolio of products and is investing in strengthening its documentation, compliance, and development processes.

Job Description

Key responsibilities:

  • Produce and maintain technical documentation in line with MDR requirements
  • Build, manage, and update Technical Files for both new and legacy products
  • Take ownership of legacy documentation, including reverse engineering and generating CAD models/drawings
  • Create production-ready, revision-controlled CAD drawings from existing products and development inputs
  • Document all design changes, improvements, and development activities
  • Ensure compliance with medical device regulations, standards, and internal gated processes
  • Support risk management activities and maintain structured design documentation (e.g. DHF)
  • Collaborate with cross-functional teams (R&D, Manufacturing, Regulatory, Supply Chain, Sales)
  • Support value engineering initiatives to improve cost efficiency without compromising quality
  • Carry out engineering change requests (ECR), including drawing/specification updates
  • Provide technical support to production teams and resolve engineering queries

The Successful Applicant

The successful candidate:

  • Minimum 5 years' experience in a technical engineering role within medical devices or a regulated environment
  • Strong understanding of Medical Device Regulation (MDR) and compliance requirements
  • Proven experience managing Technical Files, DHF, and design documentation throughout the product lifecycle
  • Strong CAD capability (SolidWorks or similar), with experience producing manufacturing-ready drawings
  • Experience working within structured product development / gated processes
  • High attention to detail with a methodical and organised approach
  • Strong communication skills with the ability to work cross-functionally
  • Analytical, proactive, and capable of managing multiple documentation streams simultaneously
  • HND (minimum) in Engineering, Product Design, or a related discipline

What's on Offer

What's on offer:

  • Salary of £42,000
  • Opportunity to play a key role in strengthening documentation and compliance within a growing medical device business
  • Exposure to both new product development and legacy product improvement projects
  • Collaborative, cross-functional working environment
  • Long-term career progression within a regulated healthcare manufacturing sector
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