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Production Engineer

Job in Greater London, London, Greater London, W1B, England, UK
Listing for: neubond
Full Time position
Listed on 2026-06-02
Job specializations:
  • Engineering
    Manufacturing Engineer, Medical Device Industry
Salary/Wage Range or Industry Benchmark: 80000 - 100000 GBP Yearly GBP 80000.00 100000.00 YEAR
Job Description & How to Apply Below
Location: Greater London

Our wearable neuromuscular devices help stroke patients rehabilitate from mobility impairments through patient-centred, more accessible, and continuous care based on deep neuroscience-driven technology. This core technology has been developed in the Neurorehabilitation Engineering Lab at Imperial College London, with support from stroke patients and clinicians in London and internationally.

Role Overview

We are looking for a hands-on Production Engineer to lead the transition of our wearable medical device from engineering prototype to scale-ready, regulatory-compliant manufacturing.

You will play a key role on establishment of manufacturing processes, including supplier selection, production line setup, and test and inspection workflows—ensuring a smooth transition from prototype to scalable volume production. You will also drive design for manufacture and assembly (DfM/DfA), implement robust quality control systems, and ensure compliance with medical device standards, delivering consistent, high-quality products ready for real-world deployment.

Key Responsibilities Manufacturing & Design Transfer
  • Lead DfM / DfA activities to support the transfer from R&D to low-volume production
  • Develop and maintain BOMs, assembly drawings, work instructions, and test procedures
  • Develop and maintain process validation, continuous improvement initiatives, and root cause analysis
  • Identify, qualify, and manage suppliers and contract manufacturers (PCBA, flex circuits, electrodes, plastics, silicone, textiles)
  • Drive cost, quality, and lead-time optimisation across the supply chain
Quality & Regulatory Support
  • Work within an ISO 13485-compliant QMS
  • Design History File (DHF)
  • Collaborate with regulatory consultants on regulatory standards (e.g., IEC 60601, risk management (ISO 14971), and usability engineering inputs)
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