Cpl in partnership with our client Pfizer are seeking a Project / CQV Engineer to join the team for an 11 month fixed term contract in Grange Castle, Dublin. Job Title: Project / CQV Engineer Department: Equipment Technology Position Reports to: 12k Engineering Cell Lead Job Purpose: Lead engineering to work together with the Capital Projects department to deliver Upgrade of CIP Skids project in Drug Substance Building. Engineer is responsible for schedule adherence, review of project design, project deliverables, close working relationship with the operational units (OpU), external vendors, design, C&Q, safety, and compliance. Engineer should have strong communication skills across the different OpUs, strong project management experience, support the technical design, create a good structure and project organisation, have Delta V expertise and strong commissioning experience for on-the-floor C&Q presence working with the team through this project phase, bringing the multiple stakeholders along. Role Requirements: The role requirements are outlined below, with suitable candidates requiring the experience and attributes specified to meet role responsibilities: Be the engineering lead for CIP project (long-term project) and work together with Capital Projects department. Ensure schedule adherence and project deliverables are achieved, working closely with OpU, Program Leads and Stakeholders, displaying the ability to meet challenging timelines within the constraints of Plan of Record, through a pro-active mindset and demonstrated innovative thinking approach to work around these, and other constraints. Strong commissioning and validation experience for active involvement in the C&Q phases and Delta V, with on-the-floor presence, bringing the different teams along. Develop and maintain relationships, systems, workstreams with your corresponding Capital Portfolio owners and all the different Operational Units. Experienced in managing capital and cashflow project, and work with capital/PM teams to manage cashflow and capital. Mindset of flexibility and fluidity to work and lead different work cells through challenging and varied project types in an ever-changing landscape. Manage, when applicable, the relationship with the A&E/Construction Management / external vendors teams through respective phases of a project. Excellent planning and project management skills. Effective motivator and communicator, a demonstrated ability to effectively influence at all levels, with a history or creating good working relationships with all departments and ability to see from all perspectives, from the OpU to other engineering departments and to other non-engineering disciplines. Embed a safety culture within the engineering team during all phases of the project lifecycle. Capable of working independently, in a well-structured manner while maintaining good communication with stakeholders & vendors. Education & Experience Requirements: Degree in an engineering or similar discipline. Minimum of 8 years engineering experience in biotechnology or pharmaceutical GMP manufacturing environment. Skills: planning skills project management skills commissioning validation communication