Senior Project Manager

1 day ago


Tuas, Singapore Grace HR Solutions Full time

Description Key Responsibilities Project Planning & ExecutionDevelop 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.Engineering CoordinationOversee engineering deliverables and interface with design teams.Review and approve technical documents, drawings, and specifications.Procurement & Contract ManagementManage procurement of equipment, materials, and services.Negotiate contracts with vendors and subcontractors.Track long-lead items and ensure timely delivery to site.Construction & Commissioning OversightSupervise 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.Client & Stakeholder ManagementAct 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.Team Leadership & ReportingLead 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.Qualifications Bachelor’s degree in Engineering, Pharmacy, or related field.7+ years of experience in project management within pharmaceutical EPCM 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.).Preferred PMP or Prince2 certification.Experience with commissioning and qualification (IQ/OQ/PQ).Familiarity with process equipment, cleanroom construction, and validation requirements. #J-18808-Ljbffr



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