CQV Lead CQV Engineer - Singapore

Role: CQV Lead / CQV Engineer 

Location: Singapore / Global Pharma Projects Industry: Pharmaceutical / Biotech / Life Sciences 

Experience: 5+ years (CQV/Validation mandatory) / CQV Lead - Team Handling Experience mandatory

Preference: Early joiners

We are looking for experienced Commissioning, Qualification & Validation (CQV) professionals to join our growing team.

Key Responsibilities:

• Lead and execute CQV activities in line with project execution plans.
• Develop and implement validation strategies, protocols, and documentation.
• Manage commissioning of HVAC, cleanrooms, API facilities, utilities, and automation systems.
• Coordinate with vendors, EPCM partners, and cross‑functional teams.
• Ensure compliance with cGMP, regulatory standards, and risk‑based validation practices.
• Review and approve test scripts (FAT/SAT/IQ/OQ/PQ).
• Drive project milestones, reporting, and stakeholder engagement.

Ideal Candidate:

• 5+ years of CQV/Validation experience in pharma/biotech projects.
• Strong knowledge of GAMP, 21 CFR Part 11, CSV, and GMP compliance.
• Proven ability to lead teams or independently execute CQV scope.
• Excellent communication and problem‑solving skills.

Interested candidates can share their CVs at [email protected]

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