Job Description

Overview

CPL Life Sciences are looking to recruit a Design Controls Engineer to join a global Pharmaceutical company based in Cambridge.

This will be a 12 month contract role (PAYE), based on site in Cambridge.

Responsibilities:

  • Lead design control and risk management activities for medical device combination product development
  • Support effective design control and risk management activities internally, at external design companies, and at related manufacturing facilities/CMOs
  • Generate and approve documentation, ensuring compliance with quality & regulatory standards (internal & external)
  • Provide support to design validation
  • Support in internal & external audits where required

    • Skills & experience:

  • Hold a relevant degree or proven experience working in a similar role
  • Understanding of working to ISO 13485/ISO 14971/21 CFR 820/21 CFR 4, and the EU Medical Devices Regulat...

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