Process Validation Engineer – (Hybrid)

Process Validation Engineer –  (Hybrid) – Tipperary 

 CREGG are now recruiting for a Process Validation Engineer (Hybrid Role) –
This is a fantastic opportunity to join a world leading Medical Device company in Tipperary as a Process Validation Engineer on a Contract basis.

Key Responsibilities:

  • Develop and/or review Process Qualifications, Test Method Validations, Gage R&R’s, Process Capability studies, Design of Experiment (DOE), and production control plans in support of product transfer.
  • Support of transfer, including the establishment of any site-specific systems/controls required for the manufacture of Scopes products at the Clonmel site.
  • Lead the translation and establishment of all Process Monitoring and activities, Acceptance Activities and inspections, and non-conforming material and product controls for the Scopes
  • Leads process improvement efforts by identifying methods to capture quality metric data and by performing appropriate analysis methods to enhance sustaining product design and new product development.
  • Coordinates and conducts technical investigation and documentation of non-conforming events and trends, and develop technical investigation
  • Be part of a strong team culture around high expectations & high performance.
  • Provide clear communication to stakeholders at key technical updates

Qualification Requirements:

  • Degree in Engineering/Quality/Science or related discipline.
  • 2-5 years’ experience in a Medical Device environment or related industry in Validation.
For more details about this role get in touch – Contact Gary Keane


Apply for this job

Job Details

10 January 2024
Job ID: 9016

Gary Keane

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