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Abbott

Makes heart devices, glucose sensors and lab tests

Facilities Engineer II

Mechanical Maintenance and Reliability EngineeringConfirmed live in the last 24 hours
Full-timeScarborough, ME, USA$61.3k - $122.7kIn-person

About the Job

Requirements

  • A bachelor's degree (BS) in Engineering, or an equivalent combination of education and experience.
  • At least 3 years of engineering experience in a manufacturing environment.
  • Working knowledge of engineering principles, methodologies, and industry standards.
  • Ability to independently troubleshoot complex equipment and system issues.
  • Experience reviewing technical documentation, including drawings, specifications, calculations, and change records.
  • Proficiency with Microsoft software, including Excel, PowerPoint, and Power BI.
  • Professionalism, integrity, accountability, respect, and commitment while representing company values and supporting organizational goals.
  • Ability to apply engineering principles to solve complex technical challenges independently with minimal supervision.
  • Initiative, ability to drive results, seek continuous learning opportunities, and maintain productivity.
  • Ability to support internal and external customers while balancing business needs, service expectations, and operational requirements.
  • Understanding of, and ability to diagnose and work effectively with, electrical and mechanical systems and equipment.
  • Ability to maintain responsibility for performance, reliability, compliance, and continuous improvement of facilities-related systems.
  • Proficiency with computer-aided design (CAD) and related engineering software to develop, modify, and maintain system layouts and documentation.
  • Ability to identify system risks, failure modes, and capacity constraints and develop mitigation strategies to support operational reliability.

Responsibilities

  • Ensure compliance with local, state, and federal agencies.
  • Manage and complete Quality Management System actions and items related to facility processes and equipment as needed.
  • Adhere to and enforce relevant safety protocols for internal staff and vendors working on projects.
  • Coordinate with other departments to define and execute project actions within established timelines.
  • Own one or more critical facilities systems, ensuring performance, compliance, and reliability throughout their lifecycle.
  • Lead root-cause investigations into complex or recurring equipment and system failures, and drive corrective and preventive actions.
  • Develop, review, and maintain facilities system standards, specifications, standard operating procedures, and design documentation.
  • Review drawings, calculations, validation documentation, and change impacts for technical accuracy and regulatory compliance.
  • Serve as the primary technical interface with vendors and contractors for assigned systems, including defining scope and making technical decisions.
  • Lead medium-scale facilities projects and system upgrades, coordinating with engineering, technicians, quality, and operations.
  • Support and lead commissioning and validation activities, including developing test strategies and analyzing data.
  • Evaluate existing systems for process suitability, capacity, and risk, and develop improvement plans as needed.
  • Manage and support change-control activities using Agile PLM or equivalent systems.
  • Provide technical guidance and informal mentorship to Facilities Engineers I and Facilities Technicians.
  • Participate in audits and inspections as a system subject matter expert.
  • Comply with U.S. Food and Drug Administration regulations, other regulatory requirements, company policies, operating procedures, processes, and task assignments.
  • Maintain cooperative communications and collaboration with employees at all levels, customers, contractors, and vendors.
  • Carry out duties in compliance with established business policies and procedures.
  • Support the development, implementation, and effectiveness of applicable quality processes in accordance with ISO, FDA, and other regulatory agencies.
  • Exhibit professional behavior in interactions with internal and external business associates, consistent with company policies and practices.
  • Understand and maintain awareness of quality consequences that may result from improper performance of assigned work.
  • Perform related tasks as requested to support the department.

Desired Qualifications

  • Prior experience working for a company operating under ISO, FDA, or similar quality systems or regulations.
  • Experience in medical device manufacturing or a related regulated industry.
  • Strong working knowledge of HVAC systems and/or manufacturing utilities.
  • Experience supporting capital projects or major system upgrades.

About the Company

Abbott

Makes heart devices, glucose sensors and lab tests

Abbott makes medical devices, diagnostic tests, nutrition products and branded generic drugs for hospitals, laboratories, pharmacies and patients. Its best-known product is the FreeStyle Libre, a coin-sized sensor worn on the upper arm that tracks blood sugar around the clock without routine finger pricks. Its other lines run from heart valves, pacemakers and brain stimulators to lab analyzers, rapid tests and mail-in colon cancer screening kits, and Abbott earns money by selling these products to health systems, labs, retailers and consumers. The company was founded in 1888 by Chicago physician Wallace Abbott and is based in Abbott Park, Illinois.

Company size
10,001+
Company stage
IPO
Headquarters
Abbott Park, IL
Founded
1888

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