Location: Beijing, China

Contract: Annual, extendable (2–3 year project)

We are hiring a CQV Manager to lead commissioning, qualification, and validation (CQV) activities for a multinational GMP facility in Beijing. This is a high-impact role in a major pharmaceutical capital project.

What You’ll Do

• Lead CQV strategy, execution, and documentation for facility, utilities, and equipment.
• Ensure compliance with FDA, EMA, ICH, and Chinese GMP standards.
• Drive coordination between engineering, construction, quality, and operations teams.
• Manage audits, inspections, and regulatory readiness.

What We’re Looking For

• 8+ years CQV experience in pharma/biotech projects.
• Proven track record in large-scale GMP facilities.
• Strong project leadership and stakeholder management skills.
• Fluent in English & Chinese (working documents in English).
• Open to candidates willing to be assigned to Beijing, China.

📌 This position is urgent and open immediately, subject to discussions and visa application if required.