Summary
The person in this temporary position will be responsible for the manufacturing of Biocare Medical’s laboratory instruments and all supporting tasks.

Essential Functions
Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

• Assembly of new and recertified production instruments:
  • Complete all instrument sub-assembly and final assembly requirements
  • Program all circuit boards, computer ports, printers, etc.
  • Calibrate instruments to required specifications
  • Flush, clean and package all completed assemblies
  • Fill daily sales orders
• Complete required quality control checks and visual inspections.
• Complete required device history record documentation.
• Preform troubleshooting, if applicable, and document action(s) taken.
• Maintain Raw Material inventory:
  • Pull parts for production in a FIFO (fist in first out) order
  • Assist with quarterly count efforts
• Daily Clean-Up:
  • Put away all QA approved assemblies and label all WIP assemblies
  • Breakdown and throw out all cardboard boxes
  • Sweep manufacturing area floors and leave walkways clear
  • Wipe down workstations and tools as needed
  • Remove any clutter
• Assist with daily Manufacturing Orders (MO’s) in Biocare’s business system, Great Plains (GP).
• Assist with department document updates: Standard Operating Procedures, Work Instructions, Assembly Forms and KPI’s.
• Other duties as assigned by Management.

Competencies

• High School Diploma or GED required, Associate Degree or higher in technical field or trade school preferred.
• Two plus (2 ) years’ experience with Electrical/Electronic and Mechanical Systems preferred.
• Two plus (2 ) years’ experience working in ISO/GMP environment preferred.
• Ability to read and follow technical instructions and drawings.
• Ability to lift up to75 pounds of force occasionally, and/or up to 25 pounds of force frequently, and/or up to 10 pounds of force constantly to move objects.
• Mechanical aptitude: possess the skills to assemble using hand and power tools.
• Understanding of Good Manufacturing Practices (GMP) and its application to the job.
• Ability to complete required production documentation.
• Basic computer skills with Word, Excel, and Outlook.
• Attention to detail and strong organizational skills.
• Ability to work in high-pressure, deadline-oriented environment.
• Ensures that all SOPs are followed and recommend Quality Improvement Measures.
• Accuracy and attention to detail.
• Familiarly with GMP, FDA and ISO regulations.

Expected Hours of Work

• 6:30 a.m. to 3:00 p.m. Monday – Friday unless otherwise determined by departments needs that may include earlier or later starting and ending hours. This position may require extended weekday or weekend hours depending on business needs.

Compensation Range

• $22 - $26 hourly