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Project Manager II - Life Sciences
Job in
Greenville, Greenville County, South Carolina, 29602, USA
Listed on 2026-08-24
Listing for:
Fluor
Full Time
position Listed on 2026-08-24
Job specializations:
-
Engineering
Regulatory Compliance Specialist
Job Description & How to Apply Below
** Short Description*
* ** Position Value Proposition*
* - Opportunity to contribute to cutting-edge pharmaceutical and biotechnology capital projects
- Exposure to advanced manufacturing, research, and cleanroom facilities
- Work within a high-growth sector with increasing investment and innovation
- Collaborate with leading clients, EPC partners, and multidisciplinary teams
- Clear path for career progression into senior project leadership roles
** 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.
This position performs project management responsibilities on small to moderate-risk engineering, procurement, fabrication, and construction/construction management (EPFC/CM) projects, or on an assigned segment of a larger project. Responsibilities include coordination of design, procurement, construction, commissioning, and startup activities.
The Project Manager II will support pharmaceutical, biotech, or life sciences capital projects, including manufacturing facilities, laboratories, and cleanroom environments. This role requires an understanding of working within regulated environments and coordinating multidisciplinary teams.
When assigned to only a segment of a larger project, this role develops a complete understanding of the contract and relevant subcontracts in order to provide full support to the project management team.
** 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
- Ability to work in a time-conscious and detail-oriented manner
- Familiarity with 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
- Collaborate in the preparation of documents required for execution of all aspects of the project in accordance with contractual obligations, Fluor's Operating System Requirements (OSR), and the Operating System Implementation Plan (OSIP)
- 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
- Other duties as assigned
** Other
Job Requirements *
* - Participate in Fluor University and other development programs for continued professional growth
- Utilize Knowledge Management processes to capture and share lessons learned and best practices
- Foster an environment that supports the development and advancement of project personnel
- Support projects by providing on-the-job mentoring, training, and leadership
- Participate in sales and marketing efforts and support proposal development when requested
- Ability to operate effectively in complex, fast-paced, and highly regulated environments
** Preferred Qualifications*
* - Experience supporting pharmaceutical, biotech, or life sciences capital projects, including manufacturing, laboratory, or cleanroom facilities
- Familiarity with GMP, FDA regulations, GAMP, and quality systems used in regulated industries
- Understanding of…
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