Scheduler

Reposted 14 Hours Ago
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Carolina, PRI
In-Office
Junior
Professional Services • Biotech • Consulting • Pharmaceutical
The Role
The Scheduler coordinates project activities, manages procurement tracking, and maintains schedules, ensuring alignment of deliverables and timelines in an FDA regulated environment.
Summary Generated by Built In

Support the Engineering and Capital Projects team by coordinating project activities, managing procurement tracking, and maintaining project schedules using Microsoft Project. This role ensures that project deliverables, timelines, and purchasing requirements are aligned, documented, and communicated effectively to both internal stakeholders and external suppliers.

Works closely with Project Managers, Project Engineers, Procurement, Maintenance, Validation, and Quality to support the successful execution of engineering projects in a regulated (FDA, cGMP) environment.

Key Responsibilities:

  • Maintain and update project schedules.
  • Track procurement activities: SAP, PRs, POs, quotes, lead times, and deliveries.
  • Coordinate with vendors, suppliers, and internal stakeholders.
  • Prepare meeting agendas, minutes, and project status reports.
  • Maintain project documentation aligned with cGMP and site procedures.



Requirements
  • Bachelor’s in Engineering, Business, Project Management, or related field.
  • 1–3 years of experience in project coordination.
  • Proficiency in SAP, MS Project, Excel, Word, PowerPoint.
  • Strong organizational and communication skills.
  • Understanding of cGMP and FDA regulatory requirements preferred.



Skills Required

  • Bachelor's in Engineering, Business, Project Management, or related field
  • 1-3 years of experience in project coordination
  • Proficiency in SAP, MS Project, Excel, Word, PowerPoint
  • Strong organizational and communication skills
  • Understanding of cGMP and FDA regulatory requirements
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The Company
0 Employees

What We Do

QRC Group specializes in providing expert consulting services in regulatory compliance, quality management, and risk management for the pharmaceuticals, medical devices, biotechnology, and other regulated industries, delivering comprehensive project management and validation solutions.

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