Validation Engineer

Cpl

Contract Engineers
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Location
Cork, County Cork, Ireland
Posted
June 25, 2026

Job Description

Objectives

To own and support validation activities in a Medical Device regulated environment.

Responsibilities

  • Own and support validation activities in a Medical Device regulated environment.
  • Responsible for assigned Process / Equipment / Facility / Utility / Software and Computer System Validation as assigned.
  • Generate Validation Plans, Protocols and Reports in support of assigned validation activity.
  • Resolution of Problems encountered during validation.
  • Ensure Consistency in validation/qualification approach across systems and projects.
  • Provide guidance and direction in the preparation and execution of validation activities
  • Be fully conversant and up to date with GMP requirements for site-wide regulatory body compliance.
  • Maintain Validation system including conducting Periodic Reviews.
  • Participate in change control processes for manufacturing Process / Equipment / Facility / Utility ...