Project Manager II

Job Description

The purpose of this position is to perform the essential job duties and functions listed below with the overall objective of establishing an execution framework that complies with the contract and ensures the safety, quality, value, timeliness, and Fluor profitability of the completed project.

• Coordination of design, procurement, construction, commissioning, and startup activities.
• Support pharmaceutical, biotech, or life sciences capital projects, including manufacturing facilities, laboratories, and cleanroom environments.
• Support execution of commissioning, qualification, and validation (CQV) activities, including coordination of IQ/OQ/PQ deliverables where applicable.
• Lead coordination across engineering, procurement, construction, quality, validation, and regulatory teams.
• Identify and manage project risks, issues, and changes in a controlled and compliant manner.
• Support the Project Director (PD) in delivering the project in accordance with execution and commercial baselines.
• Ensure effective communication with clients, contractors, and internal stakeholders in a regulated environment.

Basic Job Requirements

• Accredited four (4) year degree or global equivalent in engineering, construction management, or applicable field of study, and seven (7) years of work-related experience; or a combination of education and directly related experience equal to eleven (11) years if non-degreed.
• Ability to communicate effectively with management, coworkers, clients, vendors, contractors, and other stakeholders.
• Demonstrated knowledge of project management principles (scope, cost, schedule, risk, and change management).
• Working knowledge of applicable local, state/province, and federal/national regulations.
• Working knowledge of project management and project controls tools (e.g., Primavera P6, MS Project, cost management systems).

Long Description

• Verify with the Project Director (PD) that Health, Safety and Environmental (HSE) is emphasized throughout all phases of the project.
• Understand and support implementation of GMP, FDA, and other regulatory compliance requirements applicable to pharmaceutical projects.
• Review the Fluor contract and any relevant subcontracts.
• Prepare draft for PD approval of the project baseline, ensuring documentation is complete, maintained, and communicated to stakeholders.
• Support execution of commissioning, qualification, and validation (CQV) activities, including coordination of IQ/OQ/PQ deliverables where applicable.
• Lead coordination across engineering, procurement, construction, quality, validation, and regulatory teams.
• Identify and manage project risks, issues, and changes in a controlled and compliant manner.
• Support the PD in delivering the project in accordance with execution and commercial baselines.
• Ensure effective communication with clients, contractors, and internal stakeholders in a regulated environment.