CQV Scheduler

Platinum Global Talent Solutions•San Juan, PR

1d•Onsite

About The Position

Our client is a leading global construction consultancy renowned for delivering high-profile, complex and iconic large-scale capital projects. With a strong focus on sustainability and innovation, they are truly at the forefront of their industry. We are currently seeking a talented full-time CQV Scheduler for Life Science and Manufacturing projects. The CQV Scheduler is responsible for developing, maintaining, and optimizing commissioning, qualification, and validation schedules for large‑scale life science capital projects. This role partners closely with CQV leads, construction managers, project controls, and compliance teams to ensure system turnover and validation activities align with regulatory and project requirements.

Requirements

Scheduling experience in pharmaceutical, biotech, or medical device manufacturing.
Demonstrated experience with CQV or system turnover on major capital projects.
Proficiency with Primavera P6 and MS Project.
Strong understanding of GxP environments, system boundaries, and validation workflows.
Experience with Greenfield or Brownfield facility projects ($100M–$1B+).
Exposure to automation (DeltaV, PLCs), clean utilities, downstream/upstream processes.
Project Controls or Engineering background.

Responsibilities

Create and manage detailed CQV schedules using Primavera P6 and MS Project.
Break down all systems and equipment into System Boundary/Turnover Packages.
Sequence commissioning, IQ/OQ/PQ, cleaning validation, and regulatory readiness tasks.
Integrate engineering, procurement, construction, automation, and CQV milestones.
Track FAT/SAT, mechanical completion, commissioning readiness, and documentation workflows.
Maintain logic ties and dependencies to ensure accurate critical path.
Update weekly with field teams to capture real progress.
Analyze schedule delays and forecast impacts.
Prepare reports for project leadership, quality, and regulatory stakeholders.
Ensure schedules reflect FDA, EMA, EU Annex 15, and ISPE requirements.
Support audit readiness by ensuring documentation sequencing is correct.