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About our client: Our client is a manufacturer of offshore drilling and production equipment that is well-suited for use in deepwater applications.
About the role:
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.
About you:
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.
Other:
.Please note that only shortlisted candidates will be contacted..
Employment Agency: Kingsforce Management Services Pte. Ltd.
Employment Agency Licence No: 94C3545
EA Personnel: Kimberly Wong
EA Personnel Reg. No.: R1984508
Job ID: 139969167