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Timestamp
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1769392714
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Fetch Consultant ID
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51
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Unique ID
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e70be
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Running No
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10016
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Method
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Solo
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Edit
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No
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Frontend
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False
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Role
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Consultant
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Requestor View
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No
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Status
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Accepted
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| Who's Hiring? |
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Consultant In Charge
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Kimberly Wong
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Company Profile
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AtkinsRéalis Singapore (f.k.a Faithful + Gould)
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UEN
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198800405Z
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Client Manager
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Ker Song Sim – C – Valid
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Designation
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Director, Industrial Singapore
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Type of Placement
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Placement (Contract)
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Urgency
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Normal
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Mode of Communication
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Phone
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Visibility
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Publish
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Job Posting Date
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26/01/2026
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Posting Validity (Days)
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90
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| Job Posting Details |
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Enable AI
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No
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| Basic Details |
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Job Title
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Project Scheduler
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Job Type
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Contract
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Number of Headcount Required
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1
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Expected Date to Join
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02/03/2026
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Work Hours Per Week
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40
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Period
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Years
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No.
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2
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Salary Type
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Range
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Hide Salary
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No
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Negotiable
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Yes
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Currency
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SGD
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Min
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8,000
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Max
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12,000
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Period
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Monthly
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Add Allowance
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No
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| Entitlements |
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Work from home
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No
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Primary Work Location
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Singapore 048943
Singapore
Map It
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Classifications of Location
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Tuas / Pioneer
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Country
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Afghanistan
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| Job-Specific Details |
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Level of Competency
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Senior Position
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Years of Relevant Experience
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5
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Classification
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Non-Technical
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Sector
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Consultancy
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Project Experience
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Specialization
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- Pharmaceutical / Biotech facility projects
- Project scheduling & milestone planning
- Commissioning & Qualification (C&Q) phases
- GMP facility readiness
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Professional Characteristics
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- Strong in planning
- sequencing
- and task dependencies
- Good understanding of multi-system environments
- Detail-oriented with good critical path awareness
- Able to coordinate across engineering
- validation
- and operations teams
- Strong analytical and problem-solving skills
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Primary Responsibilities
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Scheduling, sequencing, and maintaining project milestones.
Work out the pre-requisites of all activities and manage interdependencies between systems (e.g., automation systems, utilities, and process equipment).
Coordinate and align schedules with commissioning, qualification, and production phases.
Ensure activities comply with facility requirements from commissioning to GMP status (e.g., Go Clean, Environment Monitoring).
Support engineering, commissioning, validation, and operations teams to ensure smooth project execution.
Monitor and update project schedules to reflect progress, risks, and changes.
Assist in tracking critical path activities and identifying potential bottlenecks.
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| Competencies |
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Minimum Qualifications
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Bachelor's Degree or equivalent
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Specify the Field of Study
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Yes
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Field of Study
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Language Spoken
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Language Written
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Are the Key Skills selections good enough?
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Yes
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| Summary of Key Requirements |
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Summary of Key Requirements
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- Degree in Engineering (preferably Chemical / Process), Pharmaceutical Science, Life Sciences, or related field.
- 5–7 years of relevant experience in pharmaceutical, biotech, or life sciences projects.
- Strong pharma background with experience in commissioning (SAT, IOQ), PQ, Engineering / Trial runs, and PPQ (consistency runs).
- Proven experience in project scheduling, with ability to manage multi-system projects (automation, utilities, process systems).
- Familiarity with GMP compliance and facility readiness processes.
- Strong knowledge of task dependencies, sequencing, and project milestone management.
- Excellent coordination and communication skills to work with cross-functional teams.
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Featured
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No
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On Hold
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No
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