Job Description
We are hiring a CQV Project Manager to lead commissioning, qualification, and validation projects within pharmaceutical and biotech manufacturing environments.
This role combines hands-on CQV knowledge with project leadership—owning validation execution, managing timelines, and ensuring systems are ready for GMP production.
Key Responsibilities
• Lead CQV execution across equipment, utilities, and facility systems
• Oversee IQ/OQ/PQ planning, execution, and closeout
• Manage project schedules, milestones, and deliverables
• Drive startup, system turnover, and validation readiness activities
• Coordinate with engineering, QA, operations, and vendors
• Oversee validation documentation (protocols, reports, deviations, risk assessments)
• Identify risks and ensure projects stay on track
Requirements
• 5–10+ years of experience in CQV, validati...