Serve as the primary client-side BIM and 3D model coordination lead, collaborating closely with the engineering consultant throughout the project lifecycle.
Establish, implement, and maintain BIM standards, protocols, and governance requirements across all project stakeholders.
Develop, manage, and lead the overall 3D model review, approval, and stage-gate process to ensure design quality and compliance.
Align with the engineering consultant on model area definitions, review requirements, deliverables, and review schedules.
Coordinate Agilent stakeholder participation, feedback, and decision-making during model review sessions.
Work closely with discipline leads to define and coordinate primary and secondary utility and service routing strategies.
Develop and validate first-of-a-kind or non-standard design solutions as required, securing approvals from discipline leads and end-user representatives.
Ensure accurate integration, coordination, and quality control of information and models received from third-party vendors and contractors.
Drive multidisciplinary model coordination to identify, resolve, and prevent design clashes and constructability issues.
Ensure facility designs incorporate best practices for constructability, operability, maintainability, safety, and long-term operational efficiency.
Support design decision-making by facilitating collaboration between engineering, operations, facilities, and end-user teams.
Monitor BIM and model deliverables to ensure compliance with project requirements, design standards, and project execution objectives.
Must have previously served as the 3D BIM Lead on at least one greenfield pharmaceutical capital project exceeding USD $1 billion in total installed cost.
Minimum 15 years of experience delivering large-scale pharmaceutical, life sciences, or advanced manufacturing capital projects, with significant involvement in design, engineering, construction, and project execution.
Demonstrated leadership experience managing BIM execution, multidisciplinary model coordination, and stakeholder engagement across geographically distributed project teams.
Strong understanding of pharmaceutical facility design, including GMP manufacturing, laboratories, utilities, cleanrooms, process systems, and supporting infrastructure.
Proven ability to lead global design coordination efforts involving engineering partners, contractors, equipment vendors, and owner representatives.