業務内容
You will be responsible for:
Overseeing onsite construction activities to ensure compliance with quality standards, regulatory
requirements, and specifications for CSA (Civil, Structural, Architectural) and MEP (Mechanical, Electrical, Plumbing) trades.
Developing and implementing effective quality control processes and procedures for all phases of construction.
Conducting regular inspections, audits, and reviews to identify and address quality issues promptly.
Acting as the primary liaison for quality matters, ensuring alignment between project teams, contractors, and stakeholders.
Collaborating with the construction team to resolve quality-related issues in real-time and ensure adherence to STA compliance standards.
Preparing and maintaining comprehensive quality documentation and reports to support project transparency and accountability.
Management and coordination of complex projects, with a focus on engineering, planning and design activities.
Coordinate and supervise all phases of the construction of pharmaceutical construction sites, including civil and mechanical aspects.
Manage multidisciplinary teams of technicians, suppliers and subcontractors, ensuring compliance with time and budget.
Monitor work progress and ensure compliance with quality, safety and GMP standards.
Interface with customers and stakeholders for project updates and alignments.
Analyze any critical issues and propose effective solutions to achieve objectives.
Evaluation and management of project risks, with particular attention to technical feasibility and construction sequences.
Monitoring the progress of the project, ensuring compliance with budget and timing.
Supervision on the field to ensure that implementation activities are in line with the engineering project.
応募資格
