About this role
🔹 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]
Apply with your :
Updated Resume
Notice Period
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