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Senior Facilities Project Manager (cGMP - Pharmaceutical)

DPS • Boston, MA

Posted 8 days ago

Job Snapshot

Full-Time
Degree - 4 Year Degree
£0.00 commission
£0.00 bonus
Biotechnology, Pharmaceutical
Engineering, Facilities
44

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Job Description

Senior Facilities Project Manager (cGMP - Pharmaceutical) JD817665

Boston, MA area

Summary:

DPS Engineering is looking for an accomplished Facilities Project 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.

Responsibilities:

  • 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.
  • 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.
  • Perform project management duties related to logistic planning, scope creation, project schedule and coordination.

Qualifications and Education:

  • Bachelor's degree in Mechanical Engineering or a related discipline.
  • Should have familiarity with MS Office, MS Project, SAP/Oracle, and sound accounting practices.
  • 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).
  • Strong organizational skills, oral and written communication and team attitude.
Job ID: JD817665
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