Lifecycle Validation Engineer: Periodic Review Specialist

Veg Group; Juncos (PR); On-site; USD 85,000 - 110,000; Full time

Job summary

Validation & Engineering Group, Inc. is seeking a Validation Engineer Periodic Review and Lifecycle to execute equipment periodic reviews and related lifecycle documentation for QC and QA laboratory systems.

You will collect lifecycle evidence, prepare periodic-review assessments, manage document workflows, and support the maintained validated state with on-site work and occasional non-standard hours. The role requires a Bachelor’s degree and 3+ years in a cGMP environment, with familiarity with

Qualifications

• Bachelor’s degree in Engineering, Life Sciences, or a related technical discipline.
• 3+ 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.
• Experience with Kneat, CDOCs, Maximo, LIMS, TrackWise, or equivalent systems preferred.
• Ability to work onsite and support non-standard execution hours as required.

Responsibilities

• Execute periodic reviews according to applicable procedures and approved master plans.
• Collect and evaluate equipment information, including validation and qualification history, calibration status, deviations, CAPAs, and maintenance history.
• Prepare periodic-review assessments, reports, conclusions, recommendations, and action items.
• Confirm systems remain suitable for 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.

Skills

cGMP experience

Onsite work

Flexible hours

Education

Bachelor’s degree in Engineering, Life Sciences, or related technical discipline

Tools

Kneat

CDOCs

Maximo

LIMS

TrackWise

Job description

Validation & Engineering Group, Inc. is seeking a Validation Engineer Periodic Review and Lifecycle to execute equipment periodic reviews and related lifecycle documentation for QC and QA laboratory systems.

You will collect lifecycle evidence, prepare periodic-review assessments, manage document workflows, and support the maintained validated state with on-site work and occasional non-standard hours. The role requires a Bachelor’s degree and 3+ years in a cGMP environment, with familiarity with