Engineering & Electronics

QA Validation Engineer

  • Full Time
  • Remote
  • Sligo
  • 41829927

 The QA Validation Engineer is responsible for coordination / direction and active participation in the QA validation and qualification of equipment, utilities, processes and software in compliance with clients policies, FDA, European cGMP and GAMP standards.


  • Generation/Maintenance/Execution of Project Validation Plans and schedules.
  • Generation of validation protocols and final reports to cGMP standards.
  • QA support for validation investigations and implementation of corrective actions.
  • Creation/Review/Approval of various validation and qualification documents
  • Management of validation, exception event, and change control processes.
  • Documenting all activities in line with cGMP requirements.
  • Performing cross training within the team and training of new team members.
  • Participation in continuous improvement programs to implement improvements in manufacturing, quality, safety and training systems.
  • Coordinating activities to maximize the effectiveness of all of the team members.
  • Communicating with peers and management regarding activities in the area, including elevation of events or concerns


  • Strong communication (written and oral), presentation and troubleshooting skill required
  • Effective interpersonal and organizational skills.
  • Ability to work well both independently and in a team environment.
  • Capable of prioritizing work and multitasking.


  • A third level qualification in Science, Engineering, or a relevant Quality discipline.
  • 2-4 years plus Validation/Quality experience in sterile/aseptic environment especially in the commissioning and qualification area.
  • 2-4 years plus of knowledge of cGMP and regulatory requirements relating to the pharmaceutical industry

Interested candidates should submit an up to date CV to

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