CQV Scheduler - Life Sciences
NPAworldwide, Indianapolis, IN, United States
CQV Scheduler Life Sciences
Note: This position requires the employee 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 Role
We are currently seeking a talented full-time CQV Scheduler for Life Science Construction projects. The CQV Scheduler will be 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
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.
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.
Update weekly with field teams to capture real progress.
Analyze schedule delays and forecast impacts.
Prepare reports for project leadership, quality, and regulatory stakeholders.
Ensure schedules reflect FDA, EMA, EU Annex 15, and ISPE requirements.
Support audit readiness by ensuring documentation sequencing is correct.
Qualifications
37+ 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.
We are committed to providing equal employment opportunities to all qualified individuals. We select 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.
Salary Type: Annual Salary
Salary Min: $120000
Salary Max: $170000
Currency Type: USD
#J-18808-Ljbffr
Note: This position requires the employee 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 Role
We are currently seeking a talented full-time CQV Scheduler for Life Science Construction projects. The CQV Scheduler will be 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
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.
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.
Update weekly with field teams to capture real progress.
Analyze schedule delays and forecast impacts.
Prepare reports for project leadership, quality, and regulatory stakeholders.
Ensure schedules reflect FDA, EMA, EU Annex 15, and ISPE requirements.
Support audit readiness by ensuring documentation sequencing is correct.
Qualifications
37+ 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.
We are committed to providing equal employment opportunities to all qualified individuals. We select 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.
Salary Type: Annual Salary
Salary Min: $120000
Salary Max: $170000
Currency Type: USD
#J-18808-Ljbffr