Manufacturing Engineering Support

Job Summary:

• 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.

• 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.

• Bachelor's degree in Mechanical Engineering, Manufacturing Engineering, Biomedical Engineering, Electrical Engineering, or a related technical field.