On-Site Validation Specialist (Contract) – Life Sciences

N&CS Consulting Group Inc.; Aibonito (PR); On-site; USD 65,000 - 95,000; Full time

Job summary

N&CS Consulting Group Inc. seeks a Validation Specialist for an on-site contract role based in Aibonito.

You will plan, execute, and document validation protocols for equipment, processes, and computerized systems in regulated life sciences environments. You will review validation documentation, perform test executions, analyze data, and work with engineering, manufacturing, and quality teams to ensure alignment with regulatory standards.

Qualifications

• Experience developing, executing, and documenting validation protocols.
• Experience in validation activities: qualification, performance verification, and monitoring.
• Knowledge of Quality Control practices supporting testing and data review.
• Background in Quality Assurance with audits/inspections.
• Expertise in validation principles in pharma/biotech/biologics/medical devices.
• Familiarity with FDA, EMA and GxP/ISO guidelines.
• Ability to interpret technical documentation and write clear reports.
• Bachelor's degree or equivalent experience in engineering/life sciences.
• Strong organizational skills and on-site task management.

Responsibilities

• Plan, execute, and document validation protocols for equipment, processes, and computer systems.
• Review and draft validation documentation and perform test executions.
• Analyze data and collaborate with engineering, manufacturing, and quality teams.
• Identify gaps and recommend corrective actions.
• Contribute to continuous improvement initiatives for validation and quality systems.

Skills

Computer System Validation

Process Validation

Quality Control

Quality Assurance

Regulatory guidelines

GxP

Documentation writing

Cross-functional collaboration

Report writing

On-site multitasking

Education

Bachelor's degree in engineering or life sciences

Job description

N&CS Consulting Group Inc. seeks a Validation Specialist for an on-site contract role based in Aibonito.

You will plan, execute, and document validation protocols for equipment, processes, and computerized systems in regulated life sciences environments. You will review validation documentation, perform test executions, analyze data, and work with engineering, manufacturing, and quality teams to ensure alignment with regulatory standards.