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GE HealthCare Manufacturing Engineering Intern 
United States, Kentucky 
173398849

22.09.2024
Job Description


A Manufacturing Engineering Intern is in charge of working with purchasing and validation of analytical instruments and software. Work to develop, optimize and validate analytical methods, and provide technical support for the responsible for instruments.

Responsibilities-

Key Responsibilities/Essential Functions Include:

  • Develop specifications and validate analytical instruments and software accordingly to current Good Manufacturing Practices (GMP) requirements
  • Ensure the technical support for the responsible for instruments and contribute to keep the instruments in the QC Dept in required condition at any time
  • Develop and validate new and existing analytical methods
  • Change control according to requirements
  • Ensure technical problem-solving and follow up
  • Perform repair on instruments when required
  • Develop and review procedures and methods
  • Recommend revision to methods of operation, material handling, equipment layout, or other changes to increase production or improve standards.
  • Study time, motion, methods, and speed involved in maintenance, production, and other operations to establish standard production rate and improve efficiency
  • Interpret engineering drawings, schematic diagrams, or formulas and confer with management or engineering staff to determine quality and reliability standards
  • Recommend modifications to existing quality or production standards to achieve optimum quality within limits of equipment capability
  • Evaluate data and write reports to validate or indicate deviations from existing standards.
  • Comply with EHS regulations & policies

Qualifications-


1. Specialized training in a technical area2. High school diploma or local equivalent3. Knowledge of validation work5. Technical expertise on relevant manufacturing themes


1. Bachelor degree in engineering or a technical field2. Attention to detail3. Six Sigma Green Belt certified

Quality Specific Goals:


1. Aware of and comply with the GEHC Quality Manual, Quality Management System, Quality Management Policy, Quality Goals, and applicable laws and regulations as they apply to this job type/position2. Complete all planned Quality & Compliance training within the defined deadlines3. Identify and report any quality or compliance concerns and take immediate corrective action as required4. Knowledge and understanding of Stop Orders, Concessions, ESD, Calibration, Preventative Maintenance, Material Identification & Segregation, documentation configuration control practices documentation & disposition of non-conforming material, and Good Documentation Practices requirements, as associated with this job type/position"