Validation Lead, GxP & cGMP Compliance

Hyper Recruitment Solutions Ltd; Limburg; On-site; EUR 70,000 - 110,000; Full time

Job summary

Hyper Recruitment Solutions Ltd is seeking a Senior Validation Specialist for a leading biopharmaceutical organization in the Netherlands. The role focuses on overseeing validation and qualification activities, ensuring cGMP compliance, regulatory alignment, and continuous improvement of validation processes.

You will manage URS, validation plans, and DQ/IQ/OQ/PQ deliverables, review equipment, facilities, and utilities validation, and collaborate with production and QA to drive lifecycle

Qualifications

• Degree in Engineering, Biology, Biomedical Science, Life Science or related field required.
• 5–10 years’ experience in validated GxP environments with strong validation knowledge.
• Experience managing validation lifecycle activities, risk assessments, deviations and change controls.

Responsibilities

• Oversee validation and qualification deliverables (URS, validation plans, DQ/IQ/OQ/PQ) with traceability.
• Review and approve validation documents for equipment, facilities and utilities ensuring compliance.
• Conduct periodic reviews of validated GxP assets and assess validation impact of changes.
• Support production and QA teams in validation activities and manage deviations and CAPAs.
• Contribute to continuous improvement and standardization of validation practices.

Skills

Validation

GxP

cGMP

Quality systems

Education

Bachelor's degree or higher in Engineering/Life Sciences

Tools

URS

DQ/IQ/OQ/PQ

CAPA management

Job description

Hyper Recruitment Solutions Ltd is seeking a Senior Validation Specialist for a leading biopharmaceutical organization in the Netherlands. The role focuses on overseeing validation and qualification activities, ensuring cGMP compliance, regulatory alignment, and continuous improvement of validation processes.

You will manage URS, validation plans, and DQ/IQ/OQ/PQ deliverables, review equipment, facilities, and utilities validation, and collaborate with production and QA to drive lifecycle