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2-5 Years
SGD 5,000 - 7,000 per month
  • Posted a month ago
  • Be among the first 10 applicants

Job Description

About the Role

Join our team as a CQV (Commissioning, Qualification & Validation) Engineer, supporting the start-up and validation of state-of-the-art pharmaceutical/biotech manufacturing facilities. You will work closely with project, engineering, and quality teams to ensure all systems meet GMP compliance and are ready for commercial production.

Job Responsibilities

  • Plan, execute, and manage commissioning, qualification, and validation (CQV) activities for pharmaceutical/biotech manufacturing facilities, utilities, and process equipment.
  • Develop and review CQV protocols (IQ/OQ/PQ) and reports in compliance with GMP, GAMP 5, and company procedures.
  • Coordinate with engineering, project, and quality teams to ensure timely CQV execution.
  • Troubleshoot and resolve CQV-related issues during project execution.
  • Ensure adherence to regulatory requirements (e.g., FDA, EMA, PIC/S) and local health authority guidelines.
  • Support FAT, SAT, and risk assessments for new or modified systems.
  • Provide technical input during design, construction, and operational readiness stages.

Job Requirements

  • Bachelor's degree in Engineering, Life Sciences, or related field.
  • 2-5 years of experience in commissioning/qualification/validation in pharmaceutical or biotech industries (senior roles may require 5+ years).
  • Familiar with GMP, GAMP 5, ISPE Baseline Guides, and pharmaceutical regulations.
  • Hands-on experience with utilities (e.g., WFI, clean steam, HVAC), process equipment, or cleanroom systems preferred.
  • Good communication and project coordination skills.

More Info

Job Type:
Industry:
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Job ID: 149880875

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