Validation Engineer

4 days left

03 Nov 2021
01 Dec 2021
Martin Taggart
Job Type

Validation Engineer Please remember to attach your completed Manager Approval Form for all internal applications About the Opportunity As a Validation Engineer you will be responsible for commissioning, qualification and validation activities complying with Engineering and Validation lifecycle requirements including but not limited to FAT, SAT, DR, IV, OV, IQ, OQ and PQ activities for computer systems, facilities, utilities, equipment, cleaning and sterilization.

The following activities will be included as part of your role:

  • Responsible for qualification and validation activities
  • Perform qualification and validation activities in a GMP manner aligning with site standards and industry expectations for a sterile manufacturing facility
  • Develop test scripts and execute software tests both automated and manual.
  • Develop Validation plans as required for the projects
  • Write qualification/validation protocols, execute protocols and author reports. Resolve protocol nonconformances as per site procedures
  • Present validation approach and study results to project peers and managers
  • Present and defend validation studies during regulatory inspections and internal audit
  • Generate deviations, CAPAs, perform investigations and root cause analysis
  • Perform change control assessments
  • Perform SOP revision, review and approval


  • Bachelor's degree in engineering/science and 5 years of relevant experience (e.g., engineering or quality role in a regulated environment, preferably GMP)
  • Strong interpersonal, organizational and technical skills. Capability to work both independently and in a team environment. Strong analytical and communication skills are required
  • Experience in Commissioning, qualification and Validation
  • Excellent written and verbal presentation skills to support interactions with senior leadership and inspectors are required
  • Excellent understanding of Software Development Life Cycle (SDLC).

Preferred Qualifications:

  • Familiarity with applicable HPRA, US and EU regulatory requirements
  • Excellent technical writing and verbal communication skills
  • Proficiency in Microsoft Office including Word, Excel, PowerPoint, Project and Visio
  • Knowledge of Validation Lifecycle Approach
  • Understanding of Validation using risk-based approach

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