Pharma Construction Scheduler — cGMP Master Schedule

Yonkers Industries, Inc.

Zebulon (NC)

On-site

USD 90,000 - 130,000

Full time

14 days+

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Job summary

Yonkers Industries, Inc. is seeking an experienced Construction Scheduler to support complex pharmaceutical, biotech, life-science, or process-manufacturing projects in Zebulon, NC.

The role emphasizes developing, maintaining, and communicating detailed schedules from preconstruction through validation and closeout. The candidate will collaborate with project managers, field teams, and vendors to ensure accurate sequencing, critical-path focus, and timely milestones, with strong emphasis on cGMP

Qualifications

  • 10+ years of professional construction scheduling experience.
  • Scheduling in pharmaceutical, biotech, life-science, medical-device or regulated process-manufacturing projects.
  • Strong knowledge of cGMP requirements and regulated environments.
  • Advanced proficiency in Microsoft Project and detailed, logic-driven schedules.

Responsibilities

  • Develop and maintain baseline and master project schedules from design through closeout.
  • Coordinate with project managers, field teams, vendors and clients to ensure schedules align with objectives.
  • Identify critical path, milestones, and risks; update schedules regularly.
  • Produce schedule reports, look-ahead schedules, and executive summaries.
  • Assist with schedule recovery plans when milestones are at risk.
  • Ensure schedules reflect actual site progress and changes.

Skills

Construction scheduling
MS Project
Critical path
cGMP environments

Tools

Microsoft Project

Job description

Yonkers Industries, Inc. is seeking an experienced Construction Scheduler to support complex pharmaceutical, biotech, life-science, or process-manufacturing projects in Zebulon, NC.

The role emphasizes developing, maintaining, and communicating detailed schedules from preconstruction through validation and closeout. The candidate will collaborate with project managers, field teams, and vendors to ensure accurate sequencing, critical-path focus, and timely milestones, with strong emphasis on cGMP

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