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Manufacturing Engineering Support

Blue Ash, OH
Permanent
Job Description:
  • The Manufacturing Engineering Support / Ethicon Project Support Engineer will support the development, testing, validation, and production readiness of medical device components and equipment.
  • The role involves executing and documenting test configurations, supporting equipment installation and debugging, maintaining manufacturing documentation, and collaborating with suppliers and operations teams to ensure smooth production transitions.
  • The engineer will also assist in process development, qualification activities, inventory management, and training support within a regulated medical device manufacturing environment.
Roles & Responsibilities:
  • Set up, execute, and document test configurations for components and equipment.
  • Develop, refine, and improve test procedures and protocols to enhance testing efficiency and reliability.
  • Build, maintain, and operate prototype and production equipment.
  • Support installation, startup, debugging, validation, and qualification of new products and manufacturing equipment.
  • Collaborate with suppliers, engineering, and operations teams to ensure equipment meets specifications and transitions smoothly into production.
  • Maintain and update detailed technical documentation including test results, SOPs, component specifications, and validation records.
  • Provide onboarding, training, and technical support to testing and process personnel.
  • Manage equipment and component inventory, procurement, and delivery tracking.
  • Support process development and qualification activities for components, assembly processes, and software-driven systems.
  • Ensure compliance with medical device regulations, quality standards, and manufacturing engineering best practices.
Experience:
  • 4 6 years of experience in Manufacturing Engineering Support, preferably within the medical device industry.
  • Experience supporting Ethicon or similar regulated medical device manufacturing projects is preferred.
  • Strong understanding of medical device regulations, validation processes, and manufacturing documentation practices.
  • Experience with equipment testing, troubleshooting, process qualification, and SOP development.
  • Ability to work collaboratively with cross-functional teams, suppliers, and production personnel.
  • Strong analytical, documentation, communication, and problem-solving skills.
Education:
  • Bachelor's degree in Mechanical Engineering, Manufacturing Engineering, Biomedical Engineering, Electrical Engineering, or a related technical field.

Job Type: Permanent

Job ID: 253923873