Project Engineer

Overview

A leading pharmaceutical organization in County Waterford is seeking a Project Engineer to manage various GMP facility enhancement and cleanroom construction projects within a stringent regulatory setting. This role is initially offered as a 12-month contract with potential for extension.

Primary Responsibilities

• Manage all facets of assigned projects, including scheduling, budgeting, scoping, safety, quality assurance, and adherence to regulations.
• Serve as the subject matter expert in GMP and cleanroom standards, ensuring compliance with EU GMP Annex 1 and FDA guidelines throughout projects.
• Create, update, and monitor project schedules, proactively identifying and communicating any delays.
• Ensure all project tasks are safely planned and implemented in accordance with Safe Systems of Work.

Required Qualifications and Experience

• Possess a relevant engineering degree, such as Mechanical, Chemical, Process, or a related field.
• Demonstrate proven experience delivering engineering projects within pharmaceutical or biotech GMP environments.
• Have hands-on knowledge and practical experience in cleanroom construction, commissioning, and qualification processes.

Additional Information

This role provides the opportunity to contribute significantly to regulated pharmaceutical projects with adherence to aseptic processing standards. The contract nature offers potential for extension based on project needs.