Senior CQV Scheduler
Core
Develop, monitor, and update Integrated Master Schedules (IMS) for large-scale capital programs, specifically focusing on Commissioning, Qualification, and Validation (CQV) activities in life sciences construction.
Role type
Senior CQV Scheduler (Construction/Project Controls)
Builds
Production schedules and baseline plans for life sciences facility construction projects
Domain
Life sciences construction, pharmaceutical/biotech facility development
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work -> production schedules and baseline plans
Required skills
Primavera P6, MS Project, EVM methodology, resource loading and leveling, critical path analysis, schedule variance analysis, regulatory compliance knowledge (GMP), stakeholder management, report generation
Preferred skills
Cleanroom environment familiarity, process equipment knowledge, matrix environment experience
Technologies
Primavera P6, MS Project
Responsibilities
Develop and manage detailed CQV schedules ensuring alignment with project milestones and regulatory requirements; Monitor progress of CQV tasks and implement mitigation strategies for delays; Consolidate contractor schedules into the Integrated Master Schedule; Assess impacts on critical path and report variances; Apply EVM methodology to measure project progress; Prepare schedule progress reports, trending charts, and analysis; Maintain liaison with clients and consultants; Ensure credibility of schedule information.
Seniority
Senior, hands-on IC
