Senior CQV Scheduler – Life Sciences (GxP, FDA/EMA)

NPAworldwide; Raleigh (NC); On-site; USD 140,000 - 170,000; Full time

Job summary

NPAworldwide client seeks a Senior CQV Scheduler for life science and manufacturing projects in the United States. Responsible for developing, maintaining, and optimizing commissioning and validation schedules, coordinating with construction, project controls, and compliance teams to align with regulatory and project requirements.

This full-time role requires CQV/system turnover experience, proficiency with Primavera P6 and MS Project, and strong knowledge of GxP environments and validation

Qualifications

• Scheduling experience in pharmaceutical, biotech, or medical device manufacturing.
• CQV or system turnover experience on major capital projects.
• Proficiency with Primavera P6 and MS Project.
• Strong understanding of GxP environments and validation workflows.
• Experience with Greenfield or Brownfield facilities ($100M–$1B).

Responsibilities

• Create and manage detailed CQV schedules using Primavera P6 and MS Project.
• Integrate engineering, procurement, construction, automation, and CQV milestones.
• Track FAT/SAT, commissioning readiness, and documentation workflows.
• Ensure schedules reflect regulatory requirements and audit readiness.

Skills

Scheduling experience in pharma/bioteh

CQV / system turnover

Primavera P6

MS Project

GxP/compliance knowledge

Automation exposure (DeltaV PLCs)

Tools

DeltaV

PLCs

MS Project

Primavera P6

Job description

NPAworldwide client seeks a Senior CQV Scheduler for life science and manufacturing projects in the United States. Responsible for developing, maintaining, and optimizing commissioning and validation schedules, coordinating with construction, project controls, and compliance teams to align with regulatory and project requirements.

This full-time role requires CQV/system turnover experience, proficiency with Primavera P6 and MS Project, and strong knowledge of GxP environments and validation