Validation Engineer Periodic Review… at Validation &… · Barcelone…

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

We are seeking a Validation Engineer Periodic Review and Lifecycle to execute equipment periodic reviews and related lifecycle documentation for QC and QA laboratory systems. The position will collect and evaluate lifecycle evidence, prepare periodic-review assessments, manage document workflows, and support maintenance of the validated state.

• Validation Engineer Periodic Review and Lifecycle

Key Responsibilities

• Execute periodic reviews according to applicable procedures and approved master plans.
• Collect and evaluate equipment information, including:
  • Validation and qualification history.
  • Calibration and preventive-maintenance status.
  • Deviations, CAPAs, and change controls.
  • Alarm, failure, repair, and performance history.
  • SOP and training status.
  • Previous periodic-review commitments.
  • Open actions and system improvements.
• Prepare periodic-review assessments, reports, conclusions, recommendations, and action items.
• Confirm that systems remain suitable for their intended use and in a validated state.
• Author and revise protocols, reports, SOPs, validation assessments, and supporting documents.
• Route documents through Kneat, CDOCs, or other approved document-management systems.
• Address reviewer comments and facilitate timely document approval.
• Perform protocol execution, field verification, data collection, and independent data verification.
• Support discrepancy investigations, invalid or failed runs, deviations, and corrective actions.
• Update validation master plans, equipment inventories, schedules, and deliverable trackers.
• Provide documentation and technical evidence in support of audits and inspections.
• Maintain accurate execution status and KPI information.

Qualifications

• Bachelor’s degree in Engineering, Life Sciences, or a related technical discipline.
• Three or more years of validation, qualification, quality engineering, or laboratory-equipment experience in a cGMP environment.
• Experience preparing protocols, reports, periodic reviews, validation assessments, or lifecycle documentation.
• Working knowledge of change control, deviations, CAPAs, calibration, and preventive-maintenance records.
• Experience with Kneat, CDOCs, Maximo, LIMS, TrackWise, or equivalent systems is preferred.
• Ability to work onsite and support non-standard execution hours as required.

At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.

Excited to build something meaningful together? We look forward to hearing from you.

Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.