Senior Scheduler - CQV

Turner & Townsend • Kenosha, WI

7d • Onsite

About The Position

Turner & Townsend is seeking an experienced Senior CQV Scheduler to join our team to support scheduling as a project controls function on a large-scale project. The ideal individual will have a proven track record of successfully delivering construction project control services.

Develop and manage detailed CQV (Commissioning, Qualification, and Validation) schedules for complex life sciences construction projects, ensuring alignment with project milestones and regulatory requirements. Collaborate with cross-functional teams including engineering, construction, and quality to integrate CQV activities into overall project timelines. Monitor progress of CQV tasks, identify potential delays, and proactively implement mitigation strategies to keep projects on track. Utilize scheduling tools such as Primavera P6 or MS Project to create and maintain accurate schedules and reports. Support resource planning and allocation for CQV activities across multiple concurrent projects. Ensure compliance with GMP (Good Manufacturing Practices) and other regulatory standards throughout the CQV lifecycle. Provide regular updates and reports to project stakeholders, highlighting key risks, dependencies, and progress metrics. Experience in biotech, pharmaceutical, or life sciences facility construction is required; familiarity with cleanroom environments and process equipment is a plus.

Requirements

• Bachelor’s degree in construction management, cost management, quantity surveying, engineering or field related to construction.
• Minimum 5-7 years of applicable experience.
• Direct experience working on teams within a complex matrix environment.
• Expertise using Primavera P6.
• Excellent communication skills.
• Experience in biotech, pharmaceutical, or life sciences facility construction is required.

Nice To Haves

• Familiarity with cleanroom environments and process equipment is a plus.

Responsibilities

• Develop, monitor and update owners' Project Integrated Master Schedule (IMS).
• Establish the schedule management program and deliverables to be used on large scale capital programs.
• Interface with project stakeholders as trusted advisors to provide guidance and recommendations for the project.
• Prepare baseline schedules and schedule basis documents for approval by project teams.
• Conduct schedule of resource loading and leveling.
• Consolidate contractors schedule to incorporate into IMS.
• Assess impacts on the critical path and near-critical activities and report to the project team.
• Monitor schedule deviations and variances and assist in the development of alternative methods for corrective action.
• Apply EVM methodology to measure project progress.
• Review schedules with project team members on a regular basis to ensure that accurate and timely data is incorporated into the schedule.
• Prepare and provide schedule progress reports, trending charts, and schedule analysis on a periodic basis.
• Maintain record of scope changes, trends and variances that potentially affect schedule performance.
• Assure the credibility of the information contained in the schedule.
• Maintain liaison with clients and other consultants at all projects stages.
• SOX control responsibilities may be part of this role, which are to be adhered to where applicable.
• Develop and manage detailed CQV (Commissioning, Qualification, and Validation) schedules for complex life sciences construction projects, ensuring alignment with project milestones and regulatory requirements.
• Collaborate with cross-functional teams including engineering, construction, and quality to integrate CQV activities into overall project timelines.
• Monitor progress of CQV tasks, identify potential delays, and proactively implement mitigation strategies to keep projects on track.
• Utilize scheduling tools such as Primavera P6 or MS Project to create and maintain accurate schedules and reports.
• Support resource planning and allocation for CQV activities across multiple concurrent projects.
• Ensure compliance with GMP (Good Manufacturing Practices) and other regulatory standards throughout the CQV lifecycle.
• Provide regular updates and reports to project stakeholders, highlighting key risks, dependencies, and progress metrics.

Benefits

• A great place to work, where each person has the opportunity and voice to affect change.
• We want our people to succeed both in work and life.
• To support this we promote a healthy, productive and flexible working environment that respects work-life balance.

What This Job Offers

• Job Type: Full-time
• Career Level: Senior