Ref. 1243
Project Engineer
Asset Recruitment is seeking experienced Project Engineers to join our client’s dynamic management team and support biopharmaceutical projects in the Dublin region.
The ideal candidate will bring 5+ years of experience in CGMP regulated environments along with processing equipment specification, commissioning, and operation.
This is an exciting role for a motivated engineer who thrives in on-site roles. The successful candidate will plan and execute projects, demonstrate strong communication skills and coordinate technical and project support as necessary.
Responsibilities
• Lead and manage the delivery of projects across site, ensuring compliance in terms of life cycle management, documentation, adherence to schedule, safety protocols and regulatory requirements
• Plan, execute and track the progress of projects through the design phases from inception to handover including leading the development of design and installation specifications along with commissioning plans, including site walks and system acceptance reviews.
• Lead construction project activities- day to day, vendor management / permitting /PSCS
• Create and review project engineering deliverables such as technical specifications, procurement submittals and vendor turnover documentation.
• Settle robust plans and strategies in place to manage the project lifespan
• Communicate project issues and follow-up with the right skill sets to put best solutions in place on time and within budget
• Manage vendors on site and ensure project works meet site permitting requirements – developing KPI’s and governance process for Project performance, report out and action tracking
• Identify Risks and Opportunities related to activities – work with Area Owners and SME’s to develop contingency, remediation, modification, or replacement activities.
• Ensure that all asset changes and projects have the correct assessments to ensure compliance ahead of becoming operational, including MRO requirements, risk management and business continuity impact.
• Ensure that the documentation hand over and project close out is completed in compliance with site governance processes
• Ensures effective communication throughout project lifecycle by reporting to management on project activities, and KPIs including schedule and cost adherence.
• Participates in, contributes, and influence the development of the site long range capital plan
Requirements
To excel in this role, you will more than likely have:
• A 3rd level qualification in Engineering (Chemical, Process, Mechanical or equivalent)
• 5+ years’ post grad experience.
• Project and/or operations experience within a process or biopharmaceutical cGMP regulated environment.
• Experience of processing equipment specification, commissioning, and operation.
• Demonstrated ability to work cross-functionally both at a site and global level
• Knowledge of Project and vendor management and Industry Best Practices.
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