The Power Group Ltd. has been operating since 1982 and has over 30 years of experience providing engineering and technical personnel to the Pharmaceutical, Medical Device, Electrical, Renewable Energy, and Industrial Manufacturing sectors.
We are currently seeking a Project Engineer on behalf of our client based in County Mayo. The successful candidate will join an established and high-performing Capital Projects Team and will be responsible for the delivery of a diverse portfolio of engineering projects, including equipment upgrades, process improvements, facility enhancements, infrastructure developments, and production-related capital investments within a regulated manufacturing environment.
Please see description of details below:
- Develop and maintain project plans including resource requirements, cost phasing, schedules, and production demand forecasts.
- Lead multidisciplinary engineering teams to ensure project deliverables are completed on time, within budget, and to the required quality standards.
- Develop and manage project documentation packages including Change Controls, Risk Assessments, Commissioning Documentation, Validation Protocols (FAT, SAT, IQ, OQ, PQ), and Validation Reports.
- Coordinate internal resources, contractors, vendors, and stakeholders to ensure successful project execution.
- Monitor project risks, issues, and dependencies, implementing mitigation plans where required.
- Development of Tender packages for External Companies.
- Evaluate and select vendors based on technical capability, quality standards, commercial considerations, and project requirements
- Track project expenditure and forecast costs throughout the project lifecycle
- Creation of phased costing plans.
- Provide clear guidance to team members on actions and time for completion.
- Provide feedback to management and SLT on project progress, outlining any risks or concerns.
- Ensure open communication between Projects team and Stakeholders (Internal & External)
- Completion of URS and Validation packages.
- Work with Vendors for the completion of FDS, SDS, HDS as required.
- Development of IQ, OQ, PQ protocols.
- Execution of protocols and development of validation reports.
- Assistance with the development of External Regulatory Authority documentation as required.
- Ensure that safety is the 1st priority for all project works on site.
- Ensure that GMP standards are upheld during all elements of the projects.
- Ensure that project works are completed to the highest standards and in accordance with GMP requirements, site procedures, and applicable regulatory expectations.
- Third level qualification in an Engineering or equivalent discipline/experience.
- Experience of working in Biologics, Pharmaceuticals or Medical device industry. For a minimum of 3 years experience.
- Project Engineering experience for a minimum of 2 years
- Proven track record of delivery of projects in a Multinational Organisation.
- Illustrate ability to overcome issues safety to ensure work is completed on time.
- Good communication and Interpersonal skills required to operate in a multi-function project team.
- Ability to work within a team using your own initiative to articulate and deliver tasks as required.
- Ability to work with members of various disciplines and Functions across the project