CQV Lead CQV Engineer Singapore
Job Summary
Role: CQV Lead / CQV Engineer
Location: Singapore / Global Pharma Projects Industry: Pharmaceutical / Biotech / Life Sciences
Experience: 5 years (CQV/Validation mandatory)/ CQV Lead -TeamHandling 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 crossfunctional teams.
- Ensure compliance with cGMP regulatory standards and riskbased 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 problemsolving skills.
Interested candidates can share their CVs at
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