Clean Room Assembler - 2nd Shift - Ave Maria, FL.

 Requisition ID:                       61461                          Title: Clean Room Assembler - 2nd Shift - Ave Maria, FL. Division: Arthrex Manufacturing Inc (US02) Location: Ave Maria, FL. 

 

 

 

 

 

 

Arthrex Inc. is a global medical device company and a leader in new product development and medical education in orthopedics. Arthrex Manufacturing is actively searching for a Clean Room Assembler to work at our Ave Maria, FL. Location on the Second Shift. The successful candidate will produce Quality Medical Instruments in accordance with Arthrex Manufacturing Inc. procedures and packaging processes in a safe and effective manner to meet and exceed the customer’s needs.  Ensure that production plan goals are accomplished by supporting production personnel in the assembly, inspection, and packaging of products. 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™.

 

The Clean Room is currently hiring for the Second Shift

Second - M-Th, T-Fr, 4:00pm- 2:30am, on a Rotating Crew Schedule

 

  Essential Duties and Responsibilities:

• Perform daily, monthly, and semi-annual terminal cleaning activities in the clean room.
• Perform manual and fixture assisted device assembly and packaging on medical device components, kits, convenience packs and/or any clean room specific device assembly as assigned.
• Print and apply labels onto pouches and blisters.  Assist in label reconciliation as needed.
• Perform supplemental label application, blister loading, pouch and blister sealing and visual inspection.
• Operate clean room specific equipment, automated robotic assembly equipment as needed.
• Alert of any maintenance or repair issues of any equipment or tools.
• Assist during changeovers and line setups.
• Responsible for accessing and following packaging instructions and work instructions from PLM and Document management systems based on product structure requirements.
• Inspect unit assembled and sealed for potential defects.
• Responsible for managing and segregating scrap.
• Ensure correct and complete assembly of device.
• Responsible for DHR and ERP accuracy and completion.
• Supports activities involving QC Hold and/or MRB related issues.
• 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 issues.
• Adhere to all Quality System Requirements.

 

Education/ Experience:

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