About This Role:
Provide engineering support, direction, and project management for all facilities areas, systems, and infrastructure supporting medical device manufacturing, lab, and office space. Collaborate cross-functionally to design, construct, commission, qualify, and maintain all types of manufacturing and laboratory facilities. Lead cross-discipline facilities infrastructure projects of varying sizes and timelines.
Your Responsibilities Will Include:
• Responsible for facilities space planning, facilities equipment layouts, and maximum utilization of facilities and equipment.
• Reviews and estimates design costs including construction, equipment, installation, labor, materials, preparation, and other related costs.
• Develops criteria and standards for facilities manufacturing and laboratory areas, ensuring designs meet building/safety codes.
• Developing and driving new process changes to improve efficiency and compliance.
• Coordinates with architecture/engineering firms in developing design criteria and preparing layout and detail drawings.
• Achieve detailed mechanical understanding of all infrastructure supporting medical device manufacturing and lab areas.
• Prepares bid sheets and contracts for construction projects supporting competitive bid process.
• Effectively collaborate cross-functionally in order to provide project recommendations for diverse group of customers.
• Effectively manage construction projects to tight timelines and costs
• Inspects or directs the inspection of construction and installation progress to ensure conformance to established drawings, specifications, and schedules.
• Gathers and reviews data concerning facility or equipment specifications, company or government restrictions, required completion date, and construction feasibility.
• May be responsible for scheduling, coordinating, and planning the shutdown of manufacturing areas for updates, modifications, and critical maintenance.
• Responsible 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.
What We're Looking for In You:
Required Qualifications:
• Bachelor’s degree in a technical field
• Highly self-motivated
• Proven history of leadership characteristics
• 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 fast-paced role that changes priorities quickly
Preferred Qualifications:
• Bachelor’s degree in engineering
• Experience with computer aided drafting tools
• 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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