Project Scheduler / Pharma / Up to SGD 7,500

Integrity Partners Pte. Ltd.; Singapore; On-site; SGD 80,000 - 100,000; Full time

Job summary

A leading project management firm in Singapore seeks an experienced Project Scheduler to manage complex pharmaceutical engineering project timelines. The role includes developing, maintaining schedules using Primavera P6, monitoring progress, and generating reports. Candidates must hold a relevant degree, have 5+ years in scheduling, and familiarity with GMP workflows. Expertise in Primavera P6 is mandatory. Attractive salary and benefits offered, apply with your resume to join a dynamic team.

Qualifications

• Minimum 5 years of experience in dedicated project scheduling.
• Minimum 3+ years of experience in pharmaceutical or highly regulated engineering projects.
• Strong familiarity with Good Manufacturing Practice (GMP) workflows.

Responsibilities

• Manage the end-to-end project schedule for pharmaceutical engineering projects.
• Conduct weekly progress updates and site monitoring.
• Generate comprehensive weekly/monthly status reports.

Skills

Project scheduling

Communication

Presentation

Team collaboration

Education

Bachelor’s degree in Engineering, Construction Management, or Project Management

Tools

Primavera P6

MS Project

Advanced Excel analytics

Job description

The primary objective of this role is to manage the end-to-end project schedule for complex pharmaceutical engineering projects, ensuring delivery is on time and meets stringent quality, safety, and regulatory compliance standards.

Core Deliverables

1. Project Timeline Management

   • Develop, implement, and rigorously maintain the master project schedule (Level 1–4) using Primavera P6 or MS Project.

   • Integrate and coordinate schedule inputs from all project phases: design, procurement, construction, and validation.

   • Establish and sequence all key activities based on specific pharmaceutical schedule logic and process dependencies.

2. Performance Monitoring and Control

   • Conduct weekly progress updates and site monitoring to track performance against the plan.

   • Proactively monitor the critical path and buffer time to anticipate and flag potential delays.

   • Support the development of mitigation and recovery plans to bring delayed activities back on schedule.

   • Manage and track key milestone schedules related to major equipment installation and final system validation.

3. Reporting and Analysis

   • Generate comprehensive weekly/monthly status reports and detailed 3-week lookahead schedules.

   • Provide expert scheduling input and updates during all project and client review meetings.

   • Support the technical preparation of Time Impact Analysis (TIA) and potential claims documentation.

4. Risk and Interface Coordination

   • Participate actively in project risk reviews, ensuring all schedule-related risks are documented in the risk register.

   • Coordinate seamlessly with construction, safety, and logistics teams to optimize site sequencing and workflow.

   • Interface closely with the Validation team to ensure timely achievement of IQ/OQ readiness milestones.

Essential Qualifications

• Education: Bachelor’s degree or higher in Engineering, Construction Management, or Project Management.

• Experience:

  • Minimum 5 years of experience in dedicated project scheduling.

  • Minimum 3+ years of experience in pharmaceutical or highly regulated engineering projects (preferred).

• Technical Proficiency:

  • Expert proficiency in Primavera P6 is mandatory.

  • Skilled use of MS Project and advanced Excel analytics.

• Industry Knowledge:

  • Strong familiarity with Good Manufacturing Practice (GMP) workflows and cleanroom construction sequencing.

  • Working knowledge of local construction regulations (BCA, MOM, SCDF) and site safety requirements.

• Soft Skills: Strong communication, presentation, and team collaboration skills; ability to work effectively on-site.

How to Apply:

Interested applicants may apply by sending in your updated résumé (in MS Word format) to my email or apply directly:

Consultant: Tan Jun Jie

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