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Senior Validation Engineer

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QTC Recruitment is searching for a Senior Validation Engineer to manage and oversee the site validation system, ensuring compliance with quality standards, cGMP, and regulatory requirements. The role focuses on leading qualification and validation activities, maintaining inspection readiness, and driving continuous improvement.

Details

Medical Devices

Engineering

Nijmegen - Netherlands

40 hours per week

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QTC logo icon About your role

This is how you will make the difference

Key ResponsibilitiesValidation System Management
  • Manage and maintain the site validation system in line with quality objectives.
  • Own and maintain the Validation Master Plan (VMP) and related procedures.
  • Ensure processes, materials, equipment, utilities, and facilities are qualified and validated.
  • Maintain inspection readiness for internal and external audits.
  • Ensure compliance with ISO, cGMP, and global quality standards.
Qualification & Validation Execution
  • Lead qualification and validation activities.
  • Draft and review protocols and reports (equipment, facilities, utilities, process validation/verification, cleaning validation).
  • Review TMV and CSV documentation.
  • Manage risk assessments, traceability matrices, deviations, and validation reports.
  • Oversee validation deviations and maintain VD logbook.
Monitoring & Compliance
  • Establish KPIs and monitor validation performance.
  • Develop continued process verification and annual monitoring strategies.
  • Track validation-related NCs and CAPAs to ensure timely closure.
  • Ensure ongoing GMP and regulatory compliance.
Continuous Improvement
  • Drive validation process improvements.
  • Implement best practices, tools, and technologies.
  • Promote a culture of quality and continuous improvement.

QTC logo icon what's needed

What you bring

Qualifications
  • Bachelor’s or Master’s degree in Engineering, Manufacturing, or related field.
  • Minimum 5 years of validation experience.
  • Experience with Class III sterile medical devices preferred.
  • Strong knowledge of ISO 13485, ISO 14971, cGMP, and ISPE C&Q principles.
  • Medical device or pharmaceutical industry experience preferred.
  • Project management experience.
  • Fluent in English (Dutch preferred).
  • Strong communication and organizational skills.

QTC logo icon What we offer

What's in it for you

Offer details: 
  • Competitive salary package
  • Performance-based bonus
  • Pension scheme
  • Travel allowance
  • 25+ vacation days
  • Professional development and training opportunities
  • Dynamic, international working environment

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