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****