Laser Equipment Operator - 3rd Shift - Ave Maria, FL.
ArthrexAbout the role
Arthrex, Inc. is a global medical device company and a leader in new product development and medical education. Arthrex Manufacturing is actively searching for a Laser Equipment Operator to produce Quality Medical Instruments in accordance with Arthrex Manufacturing Inc. procedures and processes in a safe and effective manner to meet and exceed the customer’s needs. Clean, assemble, laser process, inspect, and package components meeting quality requirements and the daily production schedule. Adopt an environment of continuous improvement to develop more robust procedures and improvements within existing processes to produce cost effective quality products. Join our talented team at a global medical device company focused on Helping Surgeons Treat Their Patients Better™.
If hired for this position, you will be eligible for a $2,000.00 sign-on bonus (minus appropriate tax withholdings). You will be paid the $2,000.00 during your first pay period.
This position is hiring on Third shift (10:00pm-6:30am), on Rotating Crew Schedule.
Essential Duties and Responsibilities:
- Operates Assembly, Ultrasonic Welding, Gluing, Pad Printing, Laser Marker and Laser Weld equipment in accordance with work instructions and completes setup forms.
- Inspects and verifies tools and fixtures issued to the work order are available, correct and in good repair.
- Responsible for accessing and following packaging instructions and work instructions from PLM and Document management systems based on product structure requirements.
- Performs manual device assembly using various joining processes including testing and inspection.
- Prints and applies Tags using printers for Work In Process (WIP) material.
- Verifies tags on all kitted materials and ensures tag information matches work order BOM.
- Ensures the DHR (Device History Record) is complete and accurate, including all approvals, prior to forwarding the Work Order kit for further processing.
- Promptly notifies area Coordinators and/or Supervisor of any physical inventory discrepancies, ERP and/or manufacturing systems errors or omissions, mislabeled components, missing components or other inventory anomalies.
- Performs AQL inspection in accordance with stated inspection criteria.
- Provides input for new products, processes, and fixture development.
- Ensures all departmental procedures and proper Good Manufacturing Processes (GMP) and Good Document Practices (GDP) are followed.
- Promotes a safe work environment including the use of PPE when required. Communicates issues to management that could result in process delays and/or safety is
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