DeltaV CSV Validation Engineer – Impactful GMP Compliance

No deviation

Singapore

On-site

SGD 70,000 - 110,000

Full time

14 days+

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Benefits offered by this job

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Job summary

No Deviation is seeking a Validation Engineer (CSV) to support DeltaV systems, develop and review validation protocols (IQ/OQ/PQ), and ensure regulatory compliance across the validation lifecycle.

You will collaborate with engineering and QA teams, perform risk assessments, maintain audit-ready documentation, and contribute to GMP-regulated projects with a focus on quality, integrity, and patient safety. This role offers growth in a dynamic, inclusive pharma consultancy.

Qualifications

  • Experience with DeltaV validation, coding/configuration preferred.
  • Familiarity with CSV lifecycle and GAMP 5 guidelines.
  • Strong documentation and review skills; capable of audit-ready records.

Responsibilities

  • Develop and review CSV protocols (IQ/OQ/PQ) for DeltaV systems.
  • Support configuration and validation of DeltaV automation systems.
  • Ensure compliance with GAMP 5 and regulatory guidelines.
  • Perform risk assessments and system impact assessments.
  • Review system design specifications and functional documents.
  • Coordinate testing activities and resolve validation issues.
  • Maintain proper documentation for audit readiness.

Skills

DeltaV
CSV lifecycle
GAMP 5
GMP
Documentation
Stakeholder management

Education

Degree in Engineering, IT, or related discipline

Job description

No Deviation is seeking a Validation Engineer (CSV) to support DeltaV systems, develop and review validation protocols (IQ/OQ/PQ), and ensure regulatory compliance across the validation lifecycle.

You will collaborate with engineering and QA teams, perform risk assessments, maintain audit-ready documentation, and contribute to GMP-regulated projects with a focus on quality, integrity, and patient safety. This role offers growth in a dynamic, inclusive pharma consultancy.

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