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Validation Expert

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Onsite

Validation Expert

Arcondis Group

Validation Expert

Skills

Testing & QASAP ERPITILCompliance

11 days ago

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Important information


Contract type:

Permanent

Location:

Kuala Lumpur, Federal Territory of Kuala Lumpur, Malaysia

Work mode:

Onsite

Published on:

10 October 2026

What they need


Overview The Validation Expert maintains the validated state of GxP-relevant computer systems within long-term Managed Services engagements. Working with global clients, the role applies regulatory best practices, coordinates validation activities and supports continuous improvement within a structured service-delivery model.

Key Responsibilities

  • Maintain the continuous and compliant operation of GxP-relevant computer systems within Managed Services.
  • Lead and coordinate validation and revalidation activities and maintain audit-ready lifecycle documentation.
  • Support changes, upgrades, migrations and decommissioning while preserving the validated state of systems.
  • Provide compliance support aligned with 21 CFR Part 11, 21 CFR Part 820, EudraLex and GAMP 5.
  • Collaborate with client IT, Quality and Regulatory teams on validation and compliance actions.
  • Standardise and reuse validation templates, protocols and procedures across systems and clients.
  • Monitor regulatory developments and adapt validation strategies where required.
  • Integrate validation activities with incident management, CAPA and change-control processes.
  • Work within ITIL, Agile, DevOps and Waterfall delivery approaches.

Requirements Qualifications

  • Bachelor’s degree in Computer Science, Engineering or Life Sciences.

Skills

  • Strong documentation, communication and stakeholder-collaboration skills.
  • Service-oriented approach and motivation to support improved healthcare outcomes.
  • Flexibility in working hours based on project needs.
  • Willingness to travel up to 20%.

Experience and Knowledge

  • At least 5 years of experience in Computer System Validation, IT compliance or quality assurance.
  • Strong knowledge of FDA 21 CFR Part 11 and Part 820, GAMP 5 and quality management systems in pharmaceutical or medical technology environments.
  • Experience with validated platforms such as SAP, CTMS, Veeva Vault, MES, LIMS and electronic laboratory notebooks.
  • Familiarity with ITIL-based service operations and testing-automation tools.

Advantageous

  • Master’s degree in Computer Science, Engineering, Life Sciences or a related field.

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