A leading Pharmaceutical Manufacturing site in Dublin is seeking an experienced Project Engineer to support a key capital equipment project within a GMP-regulated environment.
This role will initially focus on a major autoclave installation project, working closely with the current project lead before taking full ownership and progressing onto additional site projects over time.
Key Responsibilities
Work alongside the current project lead on an autoclave installation project
Take full ownership of the project following handover and drive it through to completion
Manage and coordinate engineering project activities from design through execution
Oversee contractor and vendor activities on-site
Ensure delivery in line with GMP and site quality standards
Support preparation of key documentation (URS, commissioning plans, validation documentation)
Collaborate with engineering, QA, validation, and operations teams
Contribute to additional capital projects across the site over time
Requirements
5–10+ years’ experience in the pharmaceutical industry
Strong background in project engineering within GMP environments
Experience working in CQV (Commissioning, Qualification & Validation)
Ideally experience with autoclave or sterile equipment installations
Strong understanding of GMP manufacturing environments
Ability to take ownership of projects following initial knowledge transfer
Strong communication and stakeholder management skills
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