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обновлено 9 дней назад

Civil Engineering Manager (Industrial Construction Manager / Site Manager)

Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
c1
Страна
Vietnam

Описание вакансии

Текст:
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TL;DR
Civil Engineering Manager (Industrial Construction Manager / Site Manager) (Industrial Construction): Managing the design, permitting, construction, and handover of a manufacturing facility with an accent on architectural, structural, civil, quality, cost, and safety coordination. Focus on coordinating designers and contractors, securing regulatory approvals, supervising construction execution, and supporting cleanroom validation and facility handover.

Location: Onsite in Hanoi City, Vietnam

Company

hirify.global develops healthcare solutions and supports manufacturing projects in the medical technology sector.

What you will do

  • Manage architectural, structural, and civil design activities across concept, basic, technical, and construction design phases.
  • Coordinate designers, project stakeholders, contractors, and authorities throughout the project lifecycle.
  • Plan and track permits, inspections, completion approvals, and regulatory documentation.
  • Supervise construction quality, cost, schedule, safety, environmental, and health requirements.
  • Coordinate technical issues, contractor evaluations, variation management, progress claims, and acceptance of completed works.
  • Support cleanroom validation, operational takeover, building handover, and defect liability management.

Requirements

  • Bachelor’s degree or higher in Civil Engineering, Construction Management, Architecture, or a related discipline.
  • 5–10 years of industrial construction experience, including at least 5 years as a Civil Engineer.
  • Proven experience with manufacturing facilities and full project lifecycle management.
  • Strong knowledge of architectural, structural, civil, and decoration works.
  • Good understanding of Vietnam construction regulations, permitting, inspections, and authority approvals.
  • Fluent spoken English is required for technical and project communication.

Nice to have

  • Experience with medical device or pharmaceutical manufacturing projects and cleanroom environments.
  • Experience supporting GMP and validation activities for cleanroom-related work packages.

Culture & Benefits

  • Work within a healthcare-focused environment centered on innovation, efficiency, sustainability, trust, transparency, and appreciation.
  • Collaborate with project, quality management, operations, procurement, design, and authority stakeholders.