Your responsibilities will include: Responsible for planning facilities equipment layouts for operational efficiency and optimal use of space and systems. Develop criteria and performance specifications for infrastructure and equipment to meet operational needs and building/safety codes. Coordinate with architecture and engineering firms to develop design criteria and technical drawings. Manage commissioning and qualification of controlled environments and utility systems supporting medical device manufacturing. Prepare bid documentation and contracts to support competitive procurement for construction projects. Collaborate cross-functionally to identify project needs and propose effective solutions. Ensure compliance of controlled areas and systems with FDA regulations, global standards, and internal procedures. Bachelor's degree in engineering or a related field Minimum of 4 years' experience in facilities engineering, project engineering, or a related discipline A proactive, self-driven approach to work and learning Demonstrated ability to lead, inspire, and support others Strong communication skills—both written and verbal Collaborative mindset with the ability to work across diverse teams and disciplines Experience navigating large, cross-functional organizations Experience leading or coordinating complex engineering design projects Ability to translate technical concepts into clear, accessible language Background working within large-scale or Fortune 500 organizations Familiarity with qualifying infrastructure for regulated manufacturing environments (e.g., medical devices) Exposure to lean manufacturing principles and continuous improvement practices Experience guiding or supporting process transformation initiatives Adaptable and resilient in dynamic, evolving environments
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