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...