Equipment Project Engineer - LTD Contractor
My client in Waterford is looking for an accountable project engineer to deliver a diverse project portfolio assignment. Delivery of this project portfolio will be within their biopharmaceutical operations which include enzyme, monoclonal antibodies (mAbs), oral dosage, medical device, laboratories & packaging operations.
The successful candidate will schedule, plan, forecast, resource, and manage all activities to ensure the project schedule, cost, quality, and scope adherence are maintained from conception to completion.
Key Responsibilities
1. Deliver on process, packaging & biopharmaceutical equipment project portfolio within our biopharmaceutical operations which include enzyme, monoclonal antibodies (mAbs), oral dosage, medical device, laboratories & packaging operations.
2. Perform procurement, acceptance of equipment & associated infrastructure, and report regularly on project status throughout the project lifecycle. Management of end-to-end project lifecycle is key to success.
3. Ensure compliance with environmental, health and safety codes, practices, approved project KPIs, performance standards, and specifications are maintained.
4. Liaise with external and internal customers, suppliers, and vendors to define and deliver right first-time project deployment.
5. Chair and interact with assigned project teams to interpret their requirements and ensure approval to align project scope as requested.
6. Assign responsibilities, mentor project team, and maintain accurate project planning documentation.
7. Communicate effectively with weekly reports to management and senior stakeholders.
8. Support other project participants to overcome obstacles when they present themselves.
9. Review engineering deliverables, initiate site change controls, and associate documentation required by the project lifecycle.
10. Responsible for delivering performance metrics for budget, schedule, scope, and quality adherence.
Essential Requirements:
1. Degree in Mechanical, Chemical, Industrial, or equivalent Engineering discipline.
2. Minimum 10+ years’ experience in a project management role.
3. Detailed knowledge of cGMP pharmaceutical environment.
4. Exemplary communication, dedication, and keen focus on delivering key to success within the role.
5. Masters an advantage.
For more information and a confidential chat, feel free to reach out to me on karl.chapple@cpl.ie or call me on 01-482 5494.
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