PE Global are recruiting for a
Project Engineer
for our pharmaceutical client based in Little Island, Cork.
This is a fully onsite role.
12-month contract role.
Job Responsibilities
Lead the delivery of Engineering projects on time, on budget & in accordance with all project & business Safety & Quality goals.
Scope new Engineering projects & secure Capital approval
Lead, support and participate in commissioning and qualification activities both current and future projects.
Updating & influencing management and project stakeholders.
Troubleshooting of process specific equipment
Coordination of the participation of specialist trades and specialist departments
Coordination of project interfaces with other projects and departments
Coordination of and interfaces with third parties (suppliers, customers, service providers, etc.)
Coordination of project documentation
Cost Estimation (creation, tracking, updating, auditing vs actual Costs, forecasting)
Project Scheduling (creation, tracking, updating, review vs current state, forecasting)
Project progress reporting & Risk Management
Constructability- & Maintainability-/Operability-studies
Project Resource Management
Checking the current condition of systems (structural, E&I as well as safety, permitting and documentation)
Organization & coordination of project meetings and appointments
Investigating and resolving Deviations raised within the Engineering Department
Provide project process and equipment related training as required.
Completion of assigned tasks projects in accordance with Change Management Procedures to support manufacture of quality medicines in accordance with cGMP and EHS requirements.
Retrospective project performance review vs project goals and lessons learned.
Participate in and lead Cross-Functional teams as necessary.
Responsible and accountable for assuring the safe accomplishment of job activities, following good environmental practices and procedures.
Commit to and demonstrate safe behavior in every activity.
Carry out routine and non-routine tasks delegated by the Manager according to appropriate procedures, values and standards.
Carry out all activities in compliance with corporate and cGMP/EHS regulatory requirements.
Compliance with Engineering and general site procedures at all times
Completion of all documentation in compliance with site procedures and GDP
Prioritize and schedule activities to support business needs and to meet requirements of Master Production Schedules
Lead and Support investigation and resolution of problems on plant.
Generate and assist with generation, review and revision of Engineering documentation as necessary.
Ensure that personal training requirements are completed in compliance with site procedures.
Support ongoing studies by Operations, Quality Validation, MSAT, Facilities and other support functions.
Education and Experience
They need to have a relevant degree (chemical, process engineering) AND a minimum of 5 years in a Project Engineering role (not C&Q or similar) from an API (active pharmaceutical ingredient) environment.
Individuals need to be able to be hands-on, proactive and able to engage with stakeholders.
Facilitate an environment of continuous improvement.
Facilitate an environment of open communication.
Lead investigations in work area as necessary.
Lead Cross-Functional project teams as necessary to support site goals.
Support training of other Operations colleagues.
Collaboration and teamwork
Initiative and motivation
Share ideas and suggestions for improvement and encourage others to do the same.
Demonstrate Credo value of integrity.
To work as a strategic partner with all other departments within the company.
Interested candidates should submit an updated CV.
Please click the link below to apply, or alternatively send an up-to-date CV
***Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in Ireland****