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 the 'Upgrade of CIP Skids' project in Drug Substance Building. Responsible for schedule adherence, review of project design, project deliverables, and maintaining a close working relationship with operational units (OpU), external vendors, design, C&Q, safety, and compliance. Possess strong communication skills across different OpUs, strong project management experience, support the technical design, create a good structure and project organization, have Delta V expertise, and strong commissioning experience for on-the-floor C&Q presence working with the team through this project phase, bringing multiple stakeholders along. Role Requirements: Be the engineering lead for the CIP project (long-term project) and work together with the 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 proactive 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, and workstreams with corresponding Capital Portfolio owners and all different Operational Units. Experienced in managing capital and cashflow projects, 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, with a demonstrated ability to effectively influence at all levels, creating good working relationships with all departments and the 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.
#J-18808-Ljbffr