Project Engineer - DPS Group Global
  • Cork, Munster, Ireland
  • via BeBee.com
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Job Description

Project Engineer role requires 5+ years experience in pharmaceutical project management, with a degree in a relevant science/engineering discipline.

The successful candidate will have a strong understanding of project management principles, including programming, scope development, design development, implementation, and project closeout.

Key responsibilities include managing project teams, executing design, procurement, construction, commissioning, and qualification phases, and ensuring a strong safety culture.

Additional requirements include experience in client-side capital projects execution, electronic change management systems, and GMP manufacturing environments.

Strong understanding of environmental, health, and safety requirements, as well as current Good Manufacturing Practices (cGMP), is also essential.

Responsibilities:

  • Manage and execute projects throughout the project life cycle from initiation to closeout.
  • Complete Front-End studies with end-users to determine the most appropriate technical solution and develop Business Cases, Budgets, and schedules.
  • Manage and execute design, procurement, construction, commissioning, and qualification phases of the project.
  • Manage cross-functional client project teams.
  • Project Scheduling & Cost Control with regular reporting to key client stakeholders.
  • Manage project changes and ensure all are captured, documented, and assessed.
  • Ensure a strong safety culture and performance in the execution of capital projects.
  • Project Validation execution.

Qualifications & Experience:

  • Experience in working in client-side Capital Projects execution role.
  • Experience in Client Electronic Change Management Systems & full end-to-end Project Lifecycle.
  • Experience in managing cross-functional teams and projects in a GMP Manufacturing Environment.
  • Understanding of Environmental, Health and Safety requirements of the pharmaceutical industry.
  • Strong understanding of the principles of current Good Manufacturing Practices (cGMP).

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