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.
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