Demo

Lead Technician, Manufacturing

Medvacon Life Sciences
Hopkins, MN Full Time
POSTED ON 2/25/2025
AVAILABLE BEFORE 4/22/2025
Important Notice: Protecting Your Information 
Medvacon Talent Acquisition only conducts initial video interviews via Microsoft Teams or Zoom. All communication will come from an email address ending in @medvacon.com. If you receive a message that seems suspicious or is not from our official domain, please report it immediately to jobs@medvacon.com. 

This is a temporary contracted position.

The Lead Automation Technician, Manufacturing-Second Shift (This position will start with first shift and likely move to a 2nd shift in a few months.  Hours for 2nd shift are 4:30pm - 1:00am) does the setup, troubleshooting and operation of manufacturing equipment and provides technical support throughout products lifecycle from product development through commercial production. 

In this role, you’ll have the opportunity to:
 
  • Lead the technical manufacturing process to include setup, calibrating and operating automated equipment. 
  • Optimize manufacturing process to minimize equipment downtime. 
  • Monitor and troubleshoot processes and machines. 
  • Work with Engineers to design, build, and test solutions to a variety of technical problems. 
  • Collect data and write daily reports for Engineering and Production. 
  • Run diagnostics and calibrate equipment, perform engineering tests, and support equipment functionality as needed.  
  • Conduct experiments and investigations in collaboration with Engineers. 
  • Order technical components and spare parts for equipment. 
To succeed in this role, you’ll need:
  • High School diploma or equivalent, and trade school certification, specialized training/apprenticeship and/or equivalent experience in high volume manufacturing automation. Automation technician certification preferred. 
  • 8 years of experience in automated manufacturing, with experience in the medical device or pharmaceutical industry preferred. 
  • 5 years of experience working with automation and packaging equipment. 
  • Experience in medical devices, pharmaceutical, GMP, or regulated industry 
  • Experience with process validation (IQ/OQ/PQ) 
  • Experience with Lean principles and metrics, problem solving methodologies, DMAIC, SPC, process capability analysis. 
  • Ability to contribute engineering support to technical plans and reports. 
  • Strong knowledge of Good Documentation (GDP) and current Good Manufacturing (GMP) Practices required. 
  • Extensive experience with developing, validating, operating, and troubleshooting automated assembly and packaging/cartoning equipment. 
  • Experience in serialization and familiarity with Drug Supply Chain Security Act (DSCSA) 
  • Background in industrial controls and PLCs. 

 

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