OT – Validation Engineer GXP systems

Panda International

JobID=J.0.12764

Junior/Intermediate CSV Specialist (GxP Systems)

Location: Geleen

Industry: Pharmaceutical / Biotechnology
Job Description Summary
We are currently seeking a Junior to Intermediate CSV Specialist to support and maintain the quality and validation of computerized systems within a GMP-regulated environment. This role focuses on ensuring compliance, system reliability, and effective support for laboratory software and infrastructure.

Key Responsibilities

  • Administer GxP computerized lab systems, including installation, backup, archiving, and data management
  • Support validation activities for computerized systems, including writing and reviewing validation protocols and reports (IQ/OQ/PQ)
  • Assist in the implementation of new systems and software
  • Provide day-to-day support to end users and troubleshoot system-related issues
  • Manage and coordinate deviations, change controls, and corrective actions
  • Ensure compliance with internal procedures and regulatory requirements
  • Collaborate with internal stakeholders to optimize system usage
  • Support audits and ensure proper follow-up on CAPAs
  • Contribute to change management processes for system updates and new implementations
  • Maintain knowledge of evolving technologies and their application

Profile

  • Bachelor’s degree in a scientific or technical field
  • Experience or strong interest in computerized systems validation (CSV)
  • Familiarity with GMP, GAMP, and data integrity principles
  • Understanding of validation practices (IQ/OQ/PQ)
  • Strong technical writing and documentation skills
  • Good communication and organizational abilities
  • Ability to work independently and in a team-oriented environment

Competencies

  • Proactive and adaptable mindset
  • Strong problem-solving skills and attention to detail
  • Collaborative and communicative approach
  • Results-driven with a focus on quality and compliance
  • Willingness to learn and grow within a regulated environment

What’s Offered

  • Entry to mid-level opportunity within a highly regulated biotech/pharma environment
  • Exposure to computerized systems and validation processes
  • A collaborative and quality-driven work culture
  • Competitive salary and development opportunities

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