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 fieldHighly self-motivatedProven history of leadership characteristicsExcellent communication skills (written and verbal)Ability to collaborate across many disciplinesComfortability working through and within changeExperience working in a large business setting across many departments and disciplinesAbility and interest in fast-paced role that changes priorities quicklyPreferred Qualifications :
Bachelor’s degree in engineeringExperience with computer aided drafting toolsExperiencing managing complex engineering design projectsAbility to distill complex topics into simplified and digestible summariesExperience working for a Fortune 500 organizationExperiencing qualifying facilities infrastructure used for medical device manufacturingExperience utilizing lean manufacturing toolsExperience driving and managing process change