Project Scheduler (Pharma Engineering Projects) | 5.5 days | Tuas

GMP Technologies; Singapore; On-site; SGD 78,000 - 123,000; Full time

Job summary

GMP Technologies is seeking a Project Scheduler for Pharma Engineering Projects in Tuas, Singapore. You will manage full-cycle project schedules across design, procurement, construction and validation to ensure timely delivery while meeting GMP, safety and quality requirements.

The role requires minimum 5 years in scheduling, with 3+ years in pharma projects. Proficiency in Primavera P6, MS Project and Excel analysis is essential; on-site work is required.

Qualifications

• Bachelor's degree or above in Engineering, Construction, or Project Management.
• Minimum 5 years in scheduling; 3+ years in pharma projects preferred.
• Proficient in Primavera P6; skilled in MS Project and Excel analytics.
• Familiar with GMP workflows and cleanroom construction sequencing.
• Knowledge of Singapore construction regulations (BCA, MOM, SCDF) and site safety requirements.
• Strong communication and team collaboration skills; able to work on-site.

Responsibilities

• Schedule Development: Develop and maintain master schedules using Primavera P6 or MS Project (Level 1-4).
• Progress Tracking & Control: Weekly update of site progress, monitoring critical paths and buffer time.
• Reporting & Communication: Prepare weekly/monthly reports and 3-week lookahead schedules; support risk reviews.

Skills

Scheduling expertise

Pharma projects

On-site collaboration

Education

Bachelor's degree in Engineering/Construction/PM

Tools

Primavera P6

MS Project

Excel analytics

Job description

Project Scheduler (Pharma Engineering Projects) | 5.5 days | Tuas

Job Openings Project Scheduler (Pharma Engineering Projects) | 5.5 days | Tuas

About the job Project Scheduler (Pharma Engineering Projects) | 5.5 days | Tuas

Purpose: To manage and control the full-cycle project schedule covering design, procurement, construction, and validation stages in a pharmaceutical engineering project. The role ensures timely project delivery under quality, safety, and compliance requirements.

Key Responsibilities

1. Schedule Development

• Develop and maintain master schedules using Primavera P6 or MS Project (Level 1-4).
• Coordinate inputs from design, procurement, construction, and validation teams.
• Sequence key activities based on pharmaceutical schedule logic and process flows.

2. Progress Tracking & Control

• Weekly update of site progress, monitoring critical paths and buffe time.
• Identify potential delays and support mitigation or recovery planning.
• Manage milestone schedules linked to equipment installation and validation.

3. Reporting & Communication

• Prepare weekly/monthly reports and 3-week lookahead schedules.
• Provide scheduling input during project and client meetings.
• Support preparation of Time Impact Analysis (TIA) and claims.
• Participate in project risk reviews, integrating schedule-related risks into the risk register.
• Work with construction, safety, and logistics teams to optimize sequencing.

5. Validation Interface (if applicable)

• Coordinate with validation team to meet IQ/OQ readiness milestones.

Requirements

• Bachelors degree or above in Engineering, Construction, or Project Management.
• Minimum 5 years in scheduling; 3+ years in pharma projects preferred.
• Proficient in Primavera P6; skilled in MS Project and Excel analytics.
• Familiar with GMP workflows and cleanroom construction sequencing.
• Knowledge of Singapore construction regulations (BCA, MOM, SCDF) and site safety requirements.
• Strong communication and team collaboration skills; able to work on-site.
• Interfaces with Design, Procurement, Construction, Validation, and Client teams

We regret that only shortlisted candidates will be notified.