Project Manager

1 week ago


Singapur, Singapore Good Job Creations (Singapore) Pte Ltd Full time

Responsibilities

  • Develop detailed project plans, schedules, and budgets.
  • Monitor project progress, identify risks, and implement mitigation strategies.
  • Ensure projects adhere to GMP and other pharmaceutical regulatory requirements.
  • Oversee engineering deliverables and interface with design teams.
  • Review and approve technical documents, drawings, and specifications.
  • Manage procurement of equipment, materials, and services.
  • Negotiate contracts with vendors and subcontractors.
  • Track long-lead items and ensure timely delivery to site.
  • Supervise construction activities, ensuring quality, safety, and schedule compliance.
  • Coordinate site inspections, testing, and commissioning activities.
  • Ensure all works are compliant with local codes and GMP standards.
  • Act as the primary interface with the client, reporting project progress.
  • Conduct regular meetings with stakeholders to align on project milestones.
  • Resolve issues and manage changes in project scope efficiently.
  • Lead project team including engineers, procurement specialists, and construction supervisors.
  • Prepare and submit periodic reports on progress, budget, risks, and KPIs.
  • Foster a culture of safety, quality, and continuous improvement.
  • Any other ad-hoc assigned.
Requirements
  • Must have 7 years of experience in project management within pharmaceutical EPCM projects.
  • Proven experience as a Project Manager in the industry building field/pharma industry construction management experience, with a track record of successfully delivering complex projects.
  • Strong knowledge of GMP, FDA, EMA, and local regulatory standards.
  • Proven experience managing multidisciplinary teams and complex projects.
  • Excellent communication, negotiation, and leadership skills.
  • Proficiency in project management tools (Primavera, MS Project, SAP, etc.).
Advantages
  • PMP or Prince2 certification.
  • Experience with commissioning and qualification (IQ/OQ/PQ).
  • Familiarity with process equipment, cleanroom construction, and validation requirements.
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