Job Details

About the job CQV Scheduler

Location: San Francisco, CA

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 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.

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:

• 3-7+ years 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 you're 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