Facilities Infrastructure Manager

17 hours ago


Arden Hills, Minnesota, United States US Tech Solutions Full time
About the Role

We are seeking a highly motivated and experienced Facilities Infrastructure Manager to join our team at US Tech Solutions. As a key member of our facilities team, you will be responsible for providing engineering support, direction, and project management for all facilities areas, systems, and infrastructure supporting medical device manufacturing, lab, and office space.

Key Responsibilities:

  • Plan and coordinate facilities equipment layouts for maximum utilization and economy of operation.
  • Review and estimate design costs, including equipment, installation, labor, materials, preparation, and other related costs.
  • Develop criteria and performance specifications for facilities infrastructure and equipment required to meet unique operating requirements and building/safety codes.
  • Develop and drive new process changes to improve efficiency and compliance.
  • Coordinate with architecture/engineering firms in developing design criteria and preparing layout and detail drawings.
  • Manage commissioning and qualification of controlled environment areas and bulk systems used in the manufacturing of medical devices.
  • Achieve detailed mechanical understanding of all infrastructure supporting medical device manufacturing and lab areas.
  • Prepare bid sheets and contracts for construction projects supporting competitive bid process.
  • Effectively collaborate cross-functionally to provide project recommendations for diverse group of customers.
  • Effectively manage construction projects to tight timelines and costs.
  • Inspect or direct the inspection of construction and installation progress to ensure conformance to established drawings, specifications, and schedules.
  • Gather and review data concerning facility or equipment specifications, company or government restrictions, required completion date, and construction feasibility.
  • May be responsible for scheduling, coordinating, and planning preventative maintenance.
  • Plan and coordinate shutdown of manufacturing areas for updates, modifications, and critical maintenance.
  • Responsible for ensuring quality compliance of controlled areas and systems in alignment with FDA regulations, global standards, site processes, and industry standards.
  • Create systematic decision assessments ranging from high-level budgetary reviews to detailed design reviews.

Requirements:

  • Bachelor's degree in engineering.
  • Must have 3+ years of experience.
  • Highly self-motivated.
  • Proven history of leadership.
  • Excellent communication skills (written and verbal).
  • Ability to collaborate across many disciplines.
  • Comfortability working through and within change.
  • Experience working in a large business setting across many departments and disciplines.
  • Ability and interest in a fast-paced role that changes priorities quickly.

Preferred Qualifications:

  • Experiencing managing complex engineering design projects.
  • Ability to distill complex topics into simplified and digestible summaries.
  • Experience working for a Fortune 500 organization.
  • Experiencing qualifying facilities infrastructure used for medical device manufacturing.
  • Experience utilizing lean manufacturing tools.
  • Experience driving and managing process change.


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