Computer System Validation Engineer

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

Job summary

Validation & Engineering Group, Inc. seeks a Computer System Validation Engineer to execute periodic reviews for ~42 computerized systems supporting QC and QA operations. You will evaluate lifecycle status, data integrity, changes, incidents, security controls, and validation documentation.

Responsibilities include planning reviews, assessing cGMP compliance, authoring reports, and supporting audits. Collaboration with Quality, IT, and lab personnel is essential for maintaining validated systems.

Qualifications

• Bachelor’s degree in Engineering, Computer Science, Information Systems, Life Sciences, or a related discipline.
• Five or more years of computerized system validation experience in pharmaceutical or biotechnology operations.
• Strong knowledge of risk-based CSV, data integrity, ALCOA+ principles, 21 CFR Part 11, and applicable GAMP practices.
• Experience conducting computerized-system periodic reviews.
• Experience with laboratory or quality platforms such as LIMS, Maximo, TrackWise, PI Historian, RIM, QBMS, or comparable systems.
• Experience preparing audit-ready documentation in Kneat, CDOCs, or equivalent platforms.

Responsibilities

• Plan and execute computerized-system periodic reviews according to approved schedules and procedures.
• Review system validation and lifecycle documentation, including intended use, configuration, validation plans, and reporting.
• Assess continued compliance with cGMP, data-integrity, and electronic-record requirements.
• Document validated-state conclusions, risks, recommendations, and remediation.
• Author and route periodic-review reports, validation assessments, and supporting documents.
• Support deviations, CAPAs, change controls, and investigations involving computerized systems.
• Collaborate with system owners, Quality, IT, Automation, and validation SMEs.
• Provide system documentation and SME support during audits and inspections.
• Maintain the review schedule, trackers, metrics, and status reports.

Skills

CSV knowledge

GxP awareness

Audits & inspections

Documentation skills

Cross-functional collaboration

Education

Bachelor’s degree (Engineering/CS/IS/Life Sciences)

Tools

LIMS

Maximo

TrackWise

PI Historian

RIM

QBMS

Kneat/CDOCs

Job description

Current job opportunities are posted here as they become available.

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 Computer System Validation Engineer to execute periodic reviews for approximately 42 computerized systems supporting QC and QA operations. The position will evaluate system lifecycle status, data integrity, changes, incidents, security controls, validation documentation, and continued fitness for intended use.

• Computer System Validation Engineer

Key Responsibilities

• Plan and execute computerized-system periodic reviews according to approved schedules and procedures.
• Review system validation and lifecycle documentation, including:
  • Intended use and current system configuration.
  • Validation plans, requirements, specifications, testing, and reports.
  • Change controls, incidents, deviations, CAPAs, and problem records.
  • User access, security roles, and periodic-access reviews.
  • Audit trails and data-integrity controls.
  • Backup, restoration, archival, and business-continuity controls.
  • Software upgrades, patches, interfaces, and infrastructure changes.
  • Vendor support and system-obsolescence status.
  • Open validation actions and previous periodic-review commitments.
• Assess continued compliance with applicable cGMP, data-integrity, and electronic-record requirements.
• Document validated-state conclusions, risks, recommendations, and required remediation.
• Author and route periodic-review reports, validation assessments, and supporting documents.
• Support deviations, CAPAs, change controls, and investigations involving computerized systems.
• Collaborate with system owners, Quality, IT, Automation, laboratory personnel, and validation SMEs.
• Provide computerized-system documentation and SME support during audits and inspections.
• Maintain the computerized-system review schedule, trackers, metrics, and status reports.

Qualifications

• Bachelor’s degree in Engineering, Computer Science, Information Systems, Life Sciences, or a related discipline.
• Five or more years of computerized system validation experience in pharmaceutical or biotechnology operations.
• Strong knowledge of risk-based CSV, data integrity, ALCOA+ principles, 21 CFR Part 11, and applicable GAMP practices.
• Experience conducting computerized-system periodic reviews.
• Experience with laboratory or quality platforms such as LIMS, Maximo, TrackWise, PI Historian, RIM, QBMS, or comparable systems.
• Experience preparing audit-ready documentation in Kneat, CDOCs, or equivalent platforms.

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.

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.