CQV Scheduler
Platinum Global Talent Solutions Ltd., San Juan, San Juan, United States
Location: San Juan, Puerto Rico
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 a talented full-time
CQV Scheduler
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
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.
#J-18808-Ljbffr
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 a talented full-time
CQV Scheduler
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
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.
#J-18808-Ljbffr