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).