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Systems Engineer (Medical and Healthcare)

EC Resourcing Limited

Bath

On-site

GBP 100,000 - 125,000

Full time

30+ days ago

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Job summary

Join a forward-thinking healthcare and diagnostics company as a Systems Engineer, where you'll lead innovative engineering solutions and drive quality improvements for medical devices. This role offers the opportunity to work on cutting-edge technologies in a collaborative environment, ensuring device integration and enhancing connectivity in the healthcare sector. With your extensive experience in engineering, you'll play a crucial role in developing new products and improving existing systems. If you're passionate about making a difference in healthcare technology, this is the perfect opportunity for you to shine.

Qualifications

  • 10+ years in healthcare or molecular engineering with FDA QSR and ISO 13485 experience.
  • Strong understanding of mechanical, electronic, and software design principles.

Responsibilities

  • Lead engineering solutions for product range and new developments.
  • Assess system architecture and recommend improvements.
  • Support regulatory submissions and lead quality improvement activities.

Skills

Project Management
Problem Solving
Technical Expertise
Molecular Biology
Statistical Analysis

Education

Bachelor’s degree in Clinical Engineering
Bachelor’s degree in Biomedical Engineering
Bachelor’s degree in Systems Engineering

Tools

Engineering Tools
Statistical Software

Job description

Systems Engineer (Medical and Healthcare)
Competitive salary - Bath - Full Time, Permanent

Our client, a healthcare and diagnostics company based near Bath, are looking for a Systems Engineer (Medical and Healthcare) to join their team.

Job Description

The Systems Engineer will lead engineering and technical insight within the company and develop engineering solutions for the existing product range and/or for new products. Additionally, the Systems Engineer will drive and oversee investigation and development activities from an engineering perspective. This person will plan and evaluate network technologies to enable, enhance, and support connectivity and integration.

This role will provide device integration engineering services to research areas, technical investigations, and clinical/technical problem-solving. The Systems Engineer will also lead quality improvement activities and suggest innovative solutions to technical problems.

Duties & Responsibilities

Responsibilities:

  • Maintain an overview of all technical aspects of the io platform and cartridges including firmware, software and system cartridge interfaces.
  • Provide technical expertise at the system level to align technical teams on hardware, and supply components.
  • Assess existing system architecture and recommend improvements and enhancements.
  • Maintain the instrument DHF.
  • Plan and lead new hardware developments and a pipeline for the io and cartridge platform.
  • Define scope of verification testing and provide key support for verification and validation activities. Complete testing protocol, analyse reports.
  • Prepare documents for and support regulatory submissions.
  • Investigate and develop solutions and new opportunities in the io and cartridge platform.
  • Monitor reliability and performance in the io platform.
  • Steer requirements for software developments on the io platform.
  • Support security management process including risk and vulnerability analysis and related documentation associated with interconnected and integrated devices and systems.
  • Interface with the R&D team to bring solutions to new and existing products including streamlining current processes and idea invention.
  • Troubleshoot and investigate errors and faults, lead root cause analysis and plan remedial actions.

To be suitable for this role, candidates will need to have the following skills and experience:

  • Bachelor’s degree in Clinical Engineering, Biomedical Engineering, Systems Engineering or related engineering field.
  • At least 10 years’ experience in health-care or molecular engineering with demonstrated experience with FDA QSR and ISO 13485.
  • Experience developing products in an IVD diagnostic development, including use of Statistics in experimental design.
  • Strong understanding of mechanical, electronic and software design principles.
  • General understanding of molecular biology, focussed on PCR and sample preparation.
  • Strong skills in management of engineering projects and/or personnel.
  • Ability to diagnose and solve technical and/or system problems of a high degree of complexity.
  • Knowledge of electronic, mechanical and/or computer reengineering design and applications principles.
  • Knowledge of clinical systems architecture used for medical device interoperability.
  • Strong level of computer literacy and the use of word processing, spreadsheets, databases, graphics, statistics, engineering tools and programming.

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