×
Register Here to Apply for Jobs or Post Jobs. X

Pharmaceutical P6 Project Scheduler

Job in Houston, Harris County, Texas, 77001, USA
Listing for: Johnson Controls
Full Time position
Listed on 2026-08-21
Job specializations:
  • Engineering
    Operations Management, Systems Engineer, Regulatory Compliance Specialist
Job Description & How to Apply Below

Join The Johnson Controls Team

Build your best future with the Johnson Controls team! As a global leader in smart, healthy, and sustainable buildings, our mission is to reimagine the performance of buildings to serve people, places, and the planet. Join a winning team that enables you to build your best future!

Our teams are uniquely positioned to support a multitude of industries across the globe. You will have the opportunity to develop yourself through meaningful work projects and learning opportunities. We strive to provide our employees with an experience focused on supporting their physical, financial, and emotional wellbeing.

Become a member of the Johnson Controls family and thrive in an empowering company culture where your voice and ideas will be heard – your next great opportunity is just a few clicks away!

What We Offer
  • Competitive base salary and a comprehensive bonus program.
  • Three weeks paid vacation in a calendar year/holidays/sick time/three PTO days in a calendar year.
  • Comprehensive benefits package including 401K, medical, dental, and vision care - available day one.
  • Extensive product and on the job/cross training opportunities
  • Encouraging and collaborative team environment
  • Dedication to safety through our Zero Harm policy
  • Providing scheduling and management support.
  • JCI Employee discount programs (The Loop by Perk Spot)
Primavera P6 Project Scheduler

The Primavera P6 Project Scheduler will develop, maintain, and analyze detailed project schedules for pharmaceutical capital projects (e.g., R&D facilities, laboratories, manufacturing plants, packaging lines, validation programs). This role ensures schedule integrity and alignment with GMP, validation, and regulatory milestones, supporting on-time delivery of highly regulated projects.

Key Responsibilities

Schedule Development & Management

  • Develop, update, and maintain detailed Primavera P6 schedules for multiple projects, including design, construction, commissioning, qualification, validation, and tech transfer activities.
  • Create and manage Work Breakdown Structures (WBS), activity coding, calendars, and resource assignments aligned with project control standards.
  • Integrate engineering, procurement, construction, CQV, and operations activities into a single, logic-driven integrated master schedule.
  • Establish and maintain baseline schedules; track progress and changes against baselines.

Schedule Analysis & Reporting

  • Perform critical path, near-critical path, and what-if scenario analyses to identify schedule risks and mitigation strategies.
  • Develop and issue regular schedule reports (dashboards, progress curves, milestone tracking, look-aheads) for project management and stakeholders.
  • Provide early warning of schedule slippage and propose recovery or acceleration plans.
  • Support schedule-related inputs for monthly project reports, stage-gate reviews, and management presentations.

Coordination & Collaboration

  • Work closely with Project Managers, Engineering, Construction, CQV, Procurement, and Operations to gather status updates and validate schedule assumptions.
  • Facilitate regular schedule review meetings and progress reviews with internal teams and external contractors.
  • Coordinate with cost control to align schedule and budget (time-phased costs, cash flow, earned value where applicable).
  • Ensure contractor and vendor schedules are integrated, consistent, and aligned with client requirements.

Pharma / GMP Focus

  • Incorporate key pharmaceutical milestones (design reviews, regulatory submissions, equipment FAT/SAT, IQ/OQ/PQ, validation, readiness for inspection, PPQ, etc.) into the integrated schedule.
  • Reflect GMP requirements, documentation deliverables, and regulatory timelines (e.g., FDA, EMA, MHRA) within the schedule logic.
  • Support readiness for regulatory inspections and audits by providing schedule evidence and documentation as required.

Governance & Continuous Improvement

  • Ensure adherence to company project controls procedures, scheduling standards, and best practices.
  • Contribute to development and refinement of scheduling templates, standards, and tools specific to pharma projects.
  • Support lessons learned exercises and implement improvements in future schedules.
Qualifications

Education

  • Bachelor's degree in engineering, Construction Management, Project Management, or related field; equivalent experience may be considered.

Experience

  • 5+ years of experience as a Project Scheduler / Planner with at least 3 years using Primavera P6.
  • Demonstrated experience on pharmaceutical, biotech, or other GMP-regulated capital projects (R&D facilities, clean rooms, manufacturing or packaging lines, utilities, etc.) strongly preferred.
  • Experience across full project lifecycle (concept through handover/validation) strongly preferred.

Technical Skills

  • Advanced proficiency in Oracle Primavera P6 (Enterprise Projects).
  • Strong understanding of critical path method (CPM) scheduling earned value principles, and project controls.
  • Proficiency with MS Excel and reporting/BI tools; experience with project…
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)
0
200
Filters
Education Level
Experience Level (years)
Posted in last:
Salary