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CSA SME

  1. United States
Ohio
  1. Contract
Competitive
  1. CAPEX Projects
33036
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CSA SME - Pharmaceuticals - 12-Month Contract - Ohio

This is a fantastic opportunity for a CSA SME to join our major, global pharmaceutical client on their latest new-build project based in Indiana, this is a large-scale greenfield capital project and investing more than $1bn.


Reporting to the Design Manager, responsibilities will be:
  • To be subject matter expert (SME) on CSA on behalf of client.
  • Coordination with the wider multi-disciplinary team for the Delivery of the project
  • Act as the Primary interface with CSA engineering providers during the Engineering and construction phase of the project.
  • Active participation in design reviews including 3D model reviews
  • Define client expectations to Architectural & Engineering designers and ensure delivery in line with this expectation, including the application of standards and guidelines.
  • Manage and ordinate interfaces between CSA design and construction with other disciplines included electrical, utilities, HVAC, Process and Mechanical.
  • Engage with Third Parties e.g. Contractors, Utility Providers, Insurers, Authorities and other Pfizer groups to ensure compliance and contribute to a successful project delivery.
  • Co-ordinate the engagement of internal and external client team members during the CSA design and construction phases
  • Ensure overall quality of the CSA design by performing regular reviews.
  • Ensure that EHS considerations are appropriately addressed throughout the Engineering phase of the project, including but not limited to HAZOP, constructability reviews and risk review studies.
  • Monitor and control Costs and changes to ensure that the project budgets are maintained

Education/Experience

To be successful in this role you will require:
  • Applicable higher education degree/diploma
  • Five or more years similar work experience exhibiting career progression
  • Computer literate with proficiency in Microsoft applications, AutoCAD etc.
  • Familiar with Navis Works and BIM 360 a significant advantage
  • Previous assignments on Pharmaceutical/Biotechnology Projects would be preferred
  • Familiar with clean room design and construction an advantage
  • Familiar with GMP manufacturing/Operations an advantage
  • Ability to use and interpret technical documents, specifications, drawings, vendor data
  • Experience in Projects from commencement to completion

If this role is of interest to you, please apply now! 

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