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Quality Engineer

Cpl Life Sciences

Cambridge, England, United Kingdom CONTRACT June 04, 2026
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Opportunity Description

Overview

12m Contract


Cambridge (2.5 days per week average on site)

We are looking for a Quality Engineer – Compliance to support medical device and combination product development programmes within a leading pharmaceutical R&D environment.


Key Responsibilities

  • Lead and support design control and risk management activities across device and combination product programmes.

  • Prepare and review Design History File (DHF) and risk management documentation.

  • Ensure compliance with quality systems and regulatory standards.

  • Support design validation activities, including human factors / usability engineering.

  • Assist with regulatory submissions, supplier assessments, and quality audits.

  • Support investigations related to clinical and commercial device manufacturing.

    • Requirements

    CONTRACT Engineers

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    Opportunity Details

    Location Cambridge, England
    Country United Kingdom
    Type CONTRACT
    Category Engineers
    Posted June 04, 2026
    Deadline July 14, 2026

    About Cpl Life Sciences

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    Cpl Life Sciences

    Cambridge, United Kingdom

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