Kerja Sepenuh Masa, CQV - Pharmaceutical Validation Engineer - West - Pharma MNC di Integrity - Maukerja

We are working with one of our clients in the pharmaceutical space, and they are recruiting for a CQV Engineer/ The candidate is responsible to ensure all systems meet GMP compliance and are ready for commercial production in plant projects.

Job Responsibilities

• Execute commissioning, qualification, and validation (CQV) activities for pharmaceutical/biotech facilities and equipment.
• Prepare and review IQ/OQ/PQ protocols and reports in compliance with GMP and GAMP 5.
• Collaborate with engineering, project, and quality teams to deliver CQV activities on schedule.
• Troubleshoot validation issues and ensure compliance with FDA, EMA, PIC/S, and other regulatory requirements.
• Support FAT, SAT, risk assessments, and project activities from design through operational readiness.

Job Requirements

• Degree in Engineering, Life Sciences, or a related field.
• 2–5 years' CQV experience in the pharmaceutical or biotech industry.
• Good knowledge of GMP, GAMP 5, ISPE, and pharmaceutical regulations.
• Experience with pharmaceutical utilities (WFI, clean steam, HVAC), process equipment, or cleanroom systems is an advantage.

How to Apply:

• Interested applicants may apply by sending in your updated résumé (in MS Word format) to my email or apply directly:
• Consultant: Tan Wei Xiang
• EA personnel reg. no.- R1658660
• EA License No. 17C8502