Laser Marking Operator-2nd Shift

• →Set up, operate, and monitor laser marking equipment to produce high-quality, permanent markings on medical device components.
• →Load and unload parts while maintaining proper part orientation and fixture alignment.
• →Verify laser marking programs and ensure correct revision levels are being used.
• →Perform first article, in-process, and final inspections to verify marking quality, readability, and location.
• →Inspect parts using microscopes, vision systems, magnification equipment, and precision measuring devices.
• →Ensure compliance with customer drawings, work instructions, manufacturing travelers, and quality standards.
• →Perform barcode and UDI verification using approved verification equipment when required.
• →Maintain complete and accurate production records, inspection results, and device history documentation.
• →Identify and segregate nonconforming products according to company procedures.
• →Troubleshoot minor equipment issues and notify maintenance or engineering of recurring problems.
• →Perform routine cleaning and preventive maintenance of laser marking equipment.
• →Maintain proper material identification and traceability throughout the manufacturing process.
• →Follow Good Manufacturing Practices (GMP), FDA regulations, ISO 13485 requirements, and company quality procedures.
• →Adhere to all safety policies, including laser safety protocols and the use of required personal protective equipment (PPE).
• →Support continuous improvement initiatives focused on quality, efficiency, and waste reduction.
• →Cross-train in other manufacturing operations as needed.

• Ability to sit or stand for extended periods.
• Frequent use of hands for handling small precision components.
• Good manual dexterity and hand-eye coordination.
• Ability to lift up to 30 pounds occasionally.
• Ability to distinguish fine details using magnification equipment.
• Ability to work in a cleanroom or controlled manufacturing environment when required.

• High school diploma or GED required.
• Technical certification in manufacturing, machining, or electronics preferred.

• 1–3 years of manufacturing experience preferred.
• Experience operating laser marking or laser engraving equipment is highly preferred.
• Experience in a medical device, aerospace, electronics, or precision manufacturing environment is preferred.
• Experience working in a regulated manufacturing environment is a plus.

• Ability to operate laser marking systems safely and efficiently.
• Ability to read and interpret engineering drawings, blueprints, and work instructions.
• Basic understanding of GD&T (Geometric Dimensioning & Tolerancing) preferred.
• Knowledge of UDI marking requirements is a plus.
• Strong attention to detail with the ability to identify cosmetic and dimensional defects.
• Experience using microscopes, vision systems, and inspection equipment.
• Ability to use precision measuring tools such as:
  • Calipers
  • Micrometers
  • Optical comparators
  • Vision inspection systems
• Basic computer skills, including production software and Microsoft Office.
• Ability to perform basic troubleshooting and identify process abnormalities.
• Excellent organizational and documentation skills.
• Ability to work independently and as part of a team.

• Manufacturing environment with laser marking equipment.
• Exposure to moving mechanical equipment and precision manufacturing processes.
• PPE required, including safety glasses and other protective equipment as necessary.
• Compliance with laser safety procedures is mandatory.
• May require overtime or weekend work to meet production schedules.

Candidates with experience operating or working around the following equipment are encouraged to apply:

• Keyence Laser Marking Systems
• Telesis Laser Markers
• Trumpf Laser Systems
• Fiber Laser Marking Equipment
• Vision Inspection Systems
• Barcode/UDI Verification Systems

• Production output meets daily scheduling requirements.
• First-pass yield and quality acceptance rates.
• Accurate UDI and product traceability compliance.
• Minimal scrap and rework.
• On-time completion of production orders.
• Accurate documentation and production records.
• Compliance with FDA, ISO 13485, GMP, and internal quality standards.