GForce Life Sciences

Director of Design And Construction

GForce Life Sciences Westchester County, NY

Direct message the job poster from GForce Life Sciences

Riley O'Connor

Riley O'Connor

Executive Recruiter at GForce Life Sciences

Consultant, Technical Director - Construction, Pharmaceutical


Summary

Our client, a Fortune 500 Pharmaceutical Company, has engaged GForce Life Sciences to provide a Technical Director of Construction. This position will report to an Associate Director of Facilities Project Management or higher, the TTCX Technical Director (TD) shall oversee quality control reviews of all drawings and specifications provided by Architects, Engineers, and other Design Professionals, as well as submittals prepared by Construction Managers, related to projects under Our clients’ Tarrytown Campus Expansion Project.


Job Duties:

  • Responsible for overseeing the owner’s quality control reviews by the Engineering, Design and Construction Department of drawings and specifications prepared by Architects, Engineers and other Design Professionals and submittals prepared by contractors for Our clients’ growing portfolio of Campus Expansion projects of new build construction
  • Performs quality control and technical reviews of Design Document milestone deliverables including drawings and specifications, as well as construction submittals.
  • Demonstrates excellence in understanding, evaluating and analyzing all areas of architectural documentation and construction detailing including exterior envelope, R&D lab design, vivaria, life safety, accessibility, other code compliance, interior detailing, materials, finishes, coordination of the trade disciplines and is considered to be a fully capable professional in these fields. Provides technical leadership for these areas for the quality control reviews by Our clients teams.
  • Coordinates with Our clients Project Managers, Engineers and other stakeholders as well as external architectural and engineering firms and Construction Managers in raising standards for quality assurance and ensuring that documents produced are coordinated and detailed correctly.
  • Coordinates scopes of work with procurement strategy and budget requirements
  • Analyzes sequence of trades, CMs means and methods and logistics plans for constructability
  • Thorough understanding of engineering systems including mechanical electrical plumbing fire protection and laboratory process systems
  • Thorough understanding of architectural building systems and products/vendor options for foundation systems, core and shell, thermal and moisture protection, building envelope, roofing, & interior construction
  • Thoroughly aware of drawing package organization, standard of care, coordination between design disciplines, level of required detail and harmonization with specifications
  • Develops the technical capabilities of Our clients’ Project Managers, Engineering Group, Architects and subject matters leads in other disciplines by implementing a plan for raising their technical capabilities as well as sharing knowledge across the business.
  • Creates Quality Assurance checklists for each phase of development of design documents (e.g. SD, DD, CD).


Mandatory Requirements

  • Bachelor's of Architecture or Engineer
  • Registered in the United States as an architect or engineer
  • Years of Experience: 7+
  • Extensive experience in pre construction doing constructability reviews of design documents
  • Skilled in the use of Microsoft Office applications (Word, Excel, Outlook, PowerPoint, etc.)
  • Preferred Software: Bluebeam Studio, AutoCAD, Revit, SharePoint


Nice to Have

  • Experience with Pharmaceutical R&D facilities


Term & Start

  • 12 Month Contract with the possibility of becoming full time
  • ASAP
  • Full time salaried Consultant
  • 4-5 days a week on site
  • Benefits included (Medical, Dental, Vision, 401k)
  • Seniority level

    Director
  • Employment type

    Contract
  • Job function

    Engineering, Design, and Project Management
  • Industries

    Construction, Biotechnology Research, and Pharmaceutical Manufacturing

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