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Facilities Manager (cGMP – Pharmaceutical) JD817695

JD817695

DPS Engineering is looking for a Facilities Manager to work with a BioPharma client in the Greater Boston, MA area. This individual will provide Project Management and support to Facility-related Projects and must have a strong understanding of GMP manufacturing environments.

Category:
Engineer Mechanical
Location:
Massachusetts
Years of Experience Req.:
7+
Date Posted:
01/01/2019
Days Remaining:
40
Employment Type:
Full-time
Education Level Req.:
Bachelors Preferred

Facilities Manager (cGMP – Pharmaceutical)              JD817695

Greater Boston, MA area                                                    

 

Summary:

 

DPS Engineering is looking for a Facilities Manager to work with a BioPharma client in the Greater Boston, MA area. This individual will provide Project Management and support to 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 operational 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.
  • Develop work plans, assign tasks, and supervise team(s).
  • Maintain and report applicable department or organiz815980.005156ational metrics.
  • Accountable for project completions and achievement of compliance goals.

 

Qualifications and Education: 

  • Bachelor’s degree in Mechanical Engineering or a related discipline.
  • 5+ 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 capital or maintenance 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 organiz815980.005156ational skills, oral and written communication and team attitude.
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