C&Q Scheduler - Pharmaceutical Capital Project

Process, Automation & Commissioning Engineers, Inc.

$100K — $120K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • 5-7 years of experience in project scheduling for C&Q or similar regulated projects.
  • Proficiency in Primavera P6 and Microsoft Project.
  • Strong knowledge of project-controls practices including baseline management and forecasting.
  • Ability to analyze and communicate schedule impacts and risks effectively.
  • Excellent coordination skills to align various scheduling activities within the project frameworks.
  • Effective written and verbal communication skills.

Responsibilities

  • Develop and maintain the integrated C&Q project schedule.
  • Perform regular updates based on progress, field execution, and document readiness.
  • Monitor key C&Q milestones and identify potential schedule risks.
  • Conduct schedule-impact analyses to inform project decision-making.
  • Align C&Q schedules with document preparation and execution phases.
  • Coordinate activities related to protocol and test script readiness.
  • Provide clear updates on schedule status and changes to project stakeholders.

Benefits

  • Opportunity to work on a major pharmaceutical capital project in Puerto Rico.
  • Gain experience in a highly regulated industry with potential for professional growth.
  • Flexible engagement as an independent consultant or contractor.
  • Collaborative work environment with multi-disciplinary project teams.
Full Job Description
About the Role

Technical & Engineering Consulting is seeking an experienced Commissioning & Qualification (C&Q) Scheduler to support a major pharmaceutical capital project in Puerto Rico.

The C&Q Scheduler will be responsible for developing, maintaining, and updating the integrated C&Q project schedule, ensuring accurate alignment between planned activities, actual progress, forecasts, document readiness, field execution, and the overall project schedule.

This position will work closely with the Project Integrator, C&Q leads, Engineering, Construction, Quality, and other project stakeholders to capture schedule updates, identify potential impacts, evaluate schedule scenarios, and provide reliable scheduling information for project decision-making.

The ideal candidate will combine strong project-controls and scheduling capabilities with an understanding of Commissioning, Qualification & Validation (CQV) activities within GMP or other highly regulated environments.
Key Responsibilities
C&Q Scheduling & Project Controls
  • Develop, maintain, and update the integrated Commissioning & Qualification (C&Q) schedule.
  • Maintain accurate plan, actual, and forecast dates for C&Q activities.
  • Perform regular schedule updates based on progress, field execution, document readiness, and project priorities.
  • Apply appropriate schedule-control practices, including:
    • Baseline management
    • Progress updates
    • Forecasting
    • Schedule-impact analysis
  • Monitor C&Q milestones, dependencies, interfaces, and critical schedule drivers.
  • Identify schedule risks, constraints, and potential delays affecting C&Q execution.
  • Escalate concerns or issues that may impact the C&Q schedule.
Schedule Analysis & Scenario Planning
  • Perform schedule-impact analyses to support C&Q reporting and project decision-making.
  • Run schedule scenarios as required to evaluate changes, constraints, sequencing, or recovery alternatives.
  • Assess and clearly communicate potential impacts to C&Q milestones and deliverables.
  • Identify schedule drivers and risks for weekly and monthly reporting.
  • Support development of schedule visuals, metrics, and other project-control information as required.
C&Q Execution & Document Readiness
  • Align the C&Q schedule with document preparation, readiness, and execution phases.
  • Coordinate scheduling activities associated with:
    • Protocol preparation and readiness
    • Test scripts
    • Field execution
    • Turnover packages
    • Deviations
    • Punch-list activities
    • Completion and closure activities
  • Ensure schedule logic appropriately reflects dependencies between documentation readiness and field execution.
  • Support alignment between C&Q activities and turnover/handshake processes.
Project Integration & Coordination
  • Work closely with the Project Integrator to ensure the latest C&Q activity updates are accurately reflected in the schedule.
  • Maintain awareness of changes to the overall project schedule and assess potential C&Q impacts.
  • Coordinate with Construction, Engineering, Quality Assurance (QA), and C&Q leads.
  • Participate in project scheduling and coordination meetings as required.
  • Provide schedule information and inputs for weekly and monthly project forums.
  • Communicate schedule status, risks, constraints, and forecast changes clearly to project stakeholders.
Minimum Qualifications
  • Demonstrated experience developing and maintaining integrated project schedules for Commissioning & Qualification (C&Q) or comparable regulated project work.
  • Proficiency with project scheduling tools such as:
    • Primavera P6
    • Microsoft Project
  • Strong understanding of scheduling and project-controls practices, including:
    • Baseline management
    • Progress measurement
    • Schedule updates
    • Forecasting
    • Schedule-impact analysis
  • Ability to analyze schedule impacts and clearly communicate key drivers, risks, and potential delays.
  • Strong coordination skills with the ability to align scheduling activities with documentation readiness and field execution.
  • Strong written and verbal communication skills.
  • Ability to prepare and communicate schedule metrics, visuals, and status information.
  • Ability to work effectively with multidisciplinary project teams in an onsite environment.
Preferred Qualifications
  • Previous experience supporting CQV deliverables within pharmaceutical, biotechnology, or other GMP-regulated environments.
  • Experience supporting turnover and handshake processes.
  • Familiarity with C&Q progress-measurement methodologies, including:
    • Protocol readiness
    • Protocol execution
    • Test-script execution
    • Deviations
    • Punch-list closure
    • Turnover readiness
  • Experience developing or supporting C&Q dashboards and progress reporting.
  • Experience coordinating directly with Construction, Engineering, QA, and C&Q organizations.
  • Previous experience supporting large pharmaceutical capital projects is highly desirable.
Technical Skills

Experience with the following is highly desirable:
  • Primavera P6
  • Microsoft Project
  • Integrated Project Scheduling
  • Commissioning & Qualification (C&Q)
  • CQV Scheduling
  • Project Controls
  • Baseline Management
  • Progress Measurement
  • Forecasting
  • Schedule Impact Analysis
  • Scenario Planning
  • C&Q Progress Reporting
  • Dashboard Reporting
  • Turnover & Handshake Processes
  • GMP / Regulated Project Environments
Position Details
  • Position: C&Q Scheduler
  • Industry: Pharmaceutical / Biotechnology / Life Sciences
  • Project: Major Pharmaceutical Capital Project
  • Work Location: Puerto Rico - Onsite
  • Work Schedule: Approximately 40 hours per week
  • Engagement: Independent Consultant / Contract
Ideal Candidate

The ideal candidate is an experienced Project Scheduler / Project Controls professional with direct exposure to Commissioning & Qualification activities in pharmaceutical or other regulated capital projects.

The candidate should understand that successful C&Q scheduling goes beyond maintaining dates in Primavera P6 or Microsoft Project. The role requires close coordination between document readiness, field execution, turnover, C&Q activities, and the integrated project schedule.

The successful candidate will be comfortable analyzing schedule scenarios, identifying risks and constraints, communicating schedule impacts to project leadership, and working collaboratively with C&Q, Construction, Engineering, Quality, and Project Management teams.

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