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Medical Devices R&D jobs

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    • Experience within medical devices or another highly regulated industry.
    • Ensure compliance with medical device design control and regulatory standards.
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    • This role focuses on advising clients on the regulatory, Quality and compliance aspects of medical devices, through a strong understanding of regulatory and…
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    • 5+ years of relevant experience in the medical device space (either industry or through consulting/service provider).
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    • Significant experience in medical device and/or drug-device combination product development;
    • This role calls for a senior engineer with substantial experience…
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    • Exposure to regulated development environments such as medical devices, automotive or other safety critical industries.
    • What skills and experience you’ll bring.
    • Improve device efficiency, stability, and manufacturability.
    • Enable affordable, scalable next-generation materials and devices.
    • Improve device efficiency, stability, and manufacturability.
    • Enable affordable, scalable next-generation materials and devices.
    • The primary purpose of this role is to leverage emerging expertise and subject matter knowledge in the development and manufacture of protein-based…
    • Experience in lab automation, medical devices, or industrial robotics.
    • Designing & creating novel electromechanical devices from scratch.
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    • This is an opportunity to register your interest in future System Validation Engineer roles within medical device development, positions that could support the…
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    • Advanced certifications in quality assurance or medical device compliance.
    • Executing system validation testing across Class III medical device development.
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    • This is an opportunity to register your interest in future System Validation Engineer roles within medical device development, positions that could support the…
  • View similar jobs with this employer
    • Advanced certifications in quality assurance or medical device compliance.
    • Executing system validation testing across Class III medical device development.
  • View similar jobs with this employer
    • Advanced certifications in quality assurance or medical device compliance.
    • Executing system validation testing across Class III medical device development.
  • View similar jobs with this employer
    • Advanced certifications in quality assurance or medical device compliance.
    • Executing system validation testing across Class III medical device development.

Job Post Details

Design Engineer - Medical Devices - job post

Gold Group
3.8 out of 5 stars
Falmouth
Up to £45,000 a year - Permanent, Full-time

Job details

Pay

  • Up to £45,000 a year

Job type

  • Permanent
  • Full-time

Location

Falmouth

Full job description

Design Engineer - Medical Devices
Falmouth, Cornwall | Site-Based

A leading global healthcare company specialising in Women's Health technologies is seeking an Design Engineer to join its growing R&D team in Cornwall. This is an excellent opportunity to work on innovative medical device development projects spanning electromechanical systems, connected devices, robotics and advanced healthcare technologies.


Candidates MUST already be based in Cornwall or willing to relocate independently.

The Opportunity

  • Join a collaborative global R&D function focused on Women's Health innovation
  • Work on new product development, product improvements and sustaining engineering activities
  • Contribute to cutting-edge technologies including electromechanical systems, connected devices and advanced medical technologies
  • Be involved across the full product lifecycle from concept through verification and validation
  • Hands-on engineering role with exposure to prototyping, testing and design activities


Key Responsibilities

  • Design and develop components, assemblies and subsystems for medical devices
  • Support new product development and engineering improvement projects
  • Develop prototypes, test methods and verification activities
  • Conduct troubleshooting, root cause analysis and technical problem solving
  • Create and maintain engineering documentation and technical reports
  • Collaborate with cross-functional engineering and project teams
  • Ensure compliance with medical device design control and regulatory standards


Requirements

  • Experience within medical devices or another highly regulated industry
  • Strong engineering design and technical problem-solving skills
  • Experience with verification & validation activities
  • Understanding of DFMA and statistical methods / DOE
  • Hands-on prototyping, testing or lab-based engineering experience
  • Experience with electromechanical, robotic or connected systems advantageous
  • Degree qualified in Engineering or related discipline


Location

  • Site-based role in Falmouth, Cornwall


Why Apply?

  • Opportunity to join a globally recognised healthcare business
  • Innovative Women's Health product portfolio
  • Collaborative R&D environment
  • Career growth within a highly technical engineering team

INDENG

Services advertised by Gold Group are those of an Agency and/or an Employment Business.
We will contact you within the next 14 days if you are selected for interview. For a copy of our privacy policy please visit our website.

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