Project / CQV Engineer

Role Summary:

• A fantastic opportunity has arisen for an experienced Project / CQV Engineer at our client’s busy biopharmaceutical site based in County Dublin.
• Lead engineering to work together with the Capital Projects department to deliver ‘Upgrade of CIP Skids’ project in Drug Substance Building.
• Engineer will be 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.
• The 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.

Core Duties and Responsibilities:

• Be the engineering lead for CIP 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.

Minimum Qualifications and Experience:

• Degree in an engineering or similar discipline.
• Minimum of 8 years engineering experience in biotechnology or pharmaceutical GMP manufacturing environment.
• Strong project management experience required
• Delta V expertise
• Strong commissioning experience for on-the-floor C&Q presence.
• Excellent communication skills

Please note, we do not require agency assistance with this role.