JOB DETAILS

Equipment & Facilities Engineer

CompanyGT Medical Technologies, Inc.
LocationRichland
Work ModeOn Site
PostedApril 18, 2026
About The Company
GT Medical Technologies was founded by a dedicated team of brain tumor specialists to address unmet needs in brain tumor treatment. The company is committed to improving the lives of patients with brain tumors through innovative solutions that elevate the standard of care. GammaTile is an FDA-cleared, bioabsorbable collagen implant embedded with radiation seeds, designed for patients with operable brain tumors. By delivering radiation directly from within—placed into the surgical cavity at the time of tumor removal—GammaTile provides immediate, localized treatment. This approach targets remaining cancer cells when they are at their lowest levels to help prevent regrowth, while minimizing radiation exposure to healthy brain tissue.(1) Since its full market launch in the United States in March 2020, GammaTile has been adopted by more than 100 leading centers, underscoring its growing acceptance in both academic and community healthcare settings. For more information, visit gammatile.com. Reference: 1. Garcia MA et al. J Neurooncol. 166:203-212 (2024).
About the Role

Description

We are seeking a skilled and motivated Equipment & Facilities Engineer to support and improve production operations in a regulated medical device manufacturing environment. This role is responsible for maintaining and enhancing equipment performance, ensuring facility readiness and compliance, and driving continuous improvement in alignment with FDA, ISO 13485, and cGMP standards.


Job Duties/Responsibilities

  • Manufacturing Equipment Support:
    • Manage preventive and corrective maintenance programs for critical manufacturing equipment and infrastructure.
    • Partner with Quality and Regulatory teams to ensure compliance with validation protocols and risk assessments.
    • Troubleshoot mechanical, electrical, pneumatic, and automated systems to minimize downtime.
    • Document changes and maintain equipment-related records per internal quality systems.
  • Facilities Engineering:
    • Oversee maintenance and operation of facility infrastructure including cleanrooms, HVAC, water systems, and critical utilities.
    • Support cleanroom compliance, including ISO Class 7/8 areas.
    • Support facility expansions, layout changes, and utility upgrades to accommodate production growth.
    • Ensure EHS and OSHA compliance for facility operations and equipment installations.
    • Manage external contractors and vendors for facility and equipment projects.
    • Assist in root cause analysis and resolution of equipment-related nonconformances and deviations.
    • Support audits and inspections by providing facility and equipment documentation and technical expertise.
    • Monitor and analyze equipment performance data to identify trends and drive continuous improvement.
    • Ensure compliance with applicable building codes, safety regulations, and environmental standards.
    • Coordinate with external contractors and vendors for facility and equipment projects.
    • Comply with Company policies and procedures.
    • Authorized to access employee and/or patient PHI and ePHI only as needed for job-related functions.
    • Other duties as assigned.

Requirements

Required Qualifications:

  • Bachelor’s Degree in Mechanical Engineering or related field or combination of education and experience totaling 8 years.
  • Hands-on experience with electromechanical equipment, automation systems, and utilities used in production environments.
  • Ability to train team members in preventative maintenance and calibration of equipment.
  • Ability to define problems, collect data, establish facts, and draw valid conclusions.
  • Excellent written and verbal communication skills.
  • Strong analytical and project management skills with the ability to manage multiple priorities.
  • Proficient in using Microsoft office programs (Outlook, Word, Excel, and PowerPoint).
  • Willingness to work a flexible schedule.
  • Able to travel for work as needed.
  • Satisfactorily pass comprehensive background screening.
  • Satisfactorily pass drug screening (if applicable to position).


Preferred Qualifications:

  • Experience supporting Class I, II, or III medical devices.
  • Six Sigma or Lean Manufacturing certification.
  • Knowledge of PLC systems.
  • Familiarity with root cause analysis (e.g., 5 Whys, Fishbone, FMEA).
  • Experience working with and around radioactive materials
  • Experience supporting a functioning class 7 cleanroom


Physical Demands/Working Conditions:

  • On-site role in a manufacturing environment.
  • May require entry into controlled environments (ISO Class 7/8 cleanrooms).
  • Occasional off-hours work to support facility or equipment projects.
  • Frequent exposure to hazardous materials requiring appropriate PPE and precautions when working with hazardous materials and chemicals.
  • Requires frequent finite hand/eye coordination.
  • Frequently picks up, carries, and moves items up to 50 lbs.
  • Some evening and weekend work depending upon workload.
  • Some overnight travel may be required for work, events, and trainings.
Key Skills
Preventive MaintenanceCorrective MaintenanceTroubleshootingMechanical SystemsElectrical SystemsPneumatic SystemsAutomated SystemsCleanroomsHVACcGMPFDA ComplianceISO 13485Root Cause AnalysisProject ManagementAnalytical SkillsEHS Compliance
Categories
EngineeringManufacturingHealthcareTrades
Job Information
📋Core Responsibilities
This role is responsible for maintaining and enhancing manufacturing equipment performance, ensuring facility readiness, and driving continuous improvement in alignment with regulatory standards. Key duties include managing maintenance programs, troubleshooting complex systems, and overseeing facility infrastructure like cleanrooms and utilities.
📋Job Type
full time
📊Experience Level
5-10
💼Company Size
101
📊Visa Sponsorship
No
💼Language
English
🏢Working Hours
40 hours
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