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Senior Utilities Project/Construction Manager (cGMP - Pharmaceutical) JD817665
Boston, MA area
DPS Engineering is looking for an accomplished Utilities Project/Construction Manager to work with a BioPharma client in the Boston, MA area. This individual will provide Project Management and support to utility and facility-related projects and must have a strong understanding of GMP manufacturing environments.
Direct the planning, design, and implementation of facilities and utilities-oriented capital projects.
Accountable for project management through the entire work flow including scope, engineering, project, commissioning, validation, and closeout.
Manage project costs, schedule and scope as it relates to quality and overall stakeholder requirements.
Balance project risk and uncertainty through risk management and mitigation plans.
Execute the planning and project management of facility-related annual shutdowns.
Perform project management duties related to logistic planning, scope creation, project schedule and coordination.
Should have demonstrated experience managing teams consisting of internal staff, supervising engineering and construction activities, and preparing turnover documentation.
Should have demonstrated project controls skills such as estimating, scheduling and cost reporting. Larger projects may require earned value/progress tracking systems.
Implement project management best practices through work plans, critical path analysis, and earned value milestones while utilizing the Project Stage Gate methodology.
Develop work plans, assign tasks, and supervise team(s).
Maintain and report applicable department or organizational metrics.
Accountable for project completions and achievement of compliance goals.
Represent department in Project Team meetings.
Qualifications and Education:
Bachelor's degree in Mechanical Engineering or a related discipline.
10+ years of pharmaceutical construction or maintenance management, and/or project management experience
Special knowledge requirements include biopharmaceutical and pharmaceutical process and facility design approaches, plus a solid understanding of cGMP requirements.
Must have strong understanding of MEP and utility systems as well as commissioning, qualification and validation activities.
Must have experience in conceptual development, design and implementation, planning and scheduling and project management of major capital projects.
Experience working to regulatory standards: FDA, Good Engineering Practice (GEP), Good Manufacturing Procedures (GMP) and Good Documentation Procedures (GDP).
Should have familiarity with MS Office, MS Project, SAP/Oracle, and sound accounting practices.
Strong organizational skills, oral and written communication and team attitude.
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