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Project Engineer

3-5 Years
SGD 4,000 - 6,000 per month
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  • Posted 14 hours ago
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Job Description

Job Scope:

  • Contribute to Life Science projects for Antaes Asia clients
  • Develop and maintain detailed C&Q schedules using project planning tools (e.g., MS Project), aligned with overall project timelines.
  • Collaborate with engineering, validation, QA, QC, and operations teams to plan and sequence commissioning and qualification activities.
  • Monitor progress, identify schedule risks, and implement mitigation strategies to ensure timely delivery of C&Q milestones.
  • Support the development and execution of C&Q strategies, including URS, DQ, IQ, OQ, and PQ documentation and activities.
  • Ensure C&Q activities comply with GMP, FDA, EMA, and other applicable regulatory standards.
  • Facilitate planning meetings, progress reviews, and reporting to project stakeholders.
  • Coordinate resource planning and availability for C&Q tasks, including vendor and contractor support.
  • Maintain accurate documentation and change control records related to C&Q scope.
  • Support audits and inspections by providing schedule-related documentation and insights.
  • Ad-hoc duties as assigned by Supervisor.
  • Contribute to the promotion of Antaes services on top of assistance provided to client.

Job Requirements:

  • Bachelor's degree in Engineering, Life Sciences, or related field.
  • Minimum 3 years of experience in project planning within a GMP-regulated pharmaceutical environment.
  • Strong understanding of C&Q processes and lifecycle documentation (URS, DQ, IQ, OQ, PQ).
  • Proficiency in project scheduling software (Primavera P6, MS Project, etc.).
  • Familiarity with ISPE Baseline Guides and industry best practices for C&Q.
  • Excellent communication, organizational, and stakeholder management skills.

Good to have:

  • PMP or equivalent project management certification.
  • Experience with large-scale pharmaceutical capital projects (e.g., new facility builds, equipment upgrades).
  • Knowledge ofcomputerized systems validation (CSV) and data integrity principles.
  • Experience with digital validation platforms (e.g. KNEAT) or eQMS systems.

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Job ID: 129852827

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