CQV Scheduler

Location: Indianapolis IN

We have similar opportunities for CQV Schedulers in multiple locations including:

Hillsboro OR / Raleigh NC / Richmond VA / Portsmouth NH / San Francisco CA / Indianapolis IN / Marietta PA / Miami FL

Note: This position requires employees to be on-site; fly in / fly out or relocation options available. Work is primarily conducted on an active construction site with heavy equipment and machinery.

About the Company

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 talented full-time CQV Schedulers for Life Science and Manufacturing projects.

Role

The CQV Scheduler is responsible for developing maintaining and optimizing commissioning qualification and validation schedules for largescale 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.

Responsibilities:

Schedule Development & Management

• 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.

Integration Across Workstreams

• 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.

Progress Tracking & Reporting

• Update weekly with field teams to capture real progress.
• Analyze schedule delays and forecast impacts.
• Prepare reports for project leadership quality and regulatory stakeholders.

Compliance & Documentation

• Ensure schedules reflect FDA EMA EU Annex 15 and ISPE requirements.
• Support audit readiness by ensuring documentation sequencing is correct.

Qualifications:

• 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.

This is an excellent opportunity for a CQV Scheduler looking to work on high-profile challenging and innovative projects. If youre an ambitious professional who thrives in a client-facing role and enjoys delivering solutions that drive project success we encourage you to apply.

Platinum Global Talent Solutions is committed to providing equal employment opportunities to all qualified individuals. We refer candidates based on their qualifications and experience without consideration of race color religion national origin sex age disability veteran status or any other legally protected status.

Why this is a Great Opportunity

• Full-time position with competitive compensation
• Comprehensive benefits including medical dental vision and 401(k)
• Opportunity to work in a client-facing role delivering significant and impactful capital projects.
• Collaborative and supportive work environment with the opportunity for growth in your career

Benefits

• Medical Dental and Vision Insurance
• Life Insurance and Accidental Death and Dismemberment
• Disability Insurance
• 401(k) plan