Facilities Engineer II

Boston Scientific•Maple Grove, MN

38d•$69,500 - $132,000

About The Position

The Facilities Engineer II will provide engineering support, strategic direction, and project management for facilities systems and infrastructure across our three Minnesota campuses, spanning medical device manufacturing, laboratory, and office environments. This role collaborates cross-functionally to design, construct, commission, qualify, and maintain all controlled environments and facility systems used in manufacturing. The Facilities Engineer II will also lead cross-disciplinary infrastructure projects of varying scope, complexity, and timelines.

Requirements

Bachelor's degree in engineering or a related field
3+ years of experience in facilities 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
Ability to travel up to 20% of the time (project-dependent)

Nice To Haves

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

Responsibilities

Responsible for planning facilities equipment layouts for economy of operation and maximum utilization of facilities and equipment.
Reviews and estimates design costs including equipment, installation, labor, materials, preparation, and other related costs.
Develops criteria and performance specifications for facilities infrastructure and equipment required to meet unique operating requirements and 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.
Manages 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.
Prepares bid sheets and contracts for construction projects supporting competitive bid process.
Effectively collaborate cross-functionally to provide project recommendations for diverse groups 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 preventative maintenance.
Plans and coordinates 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