QRC Group, LLC is a firm dedicated to offer services to the Pharmaceutical, Medical Devices and Chemical Industries in the validation and regulatory fields.

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SUMMARY 
Independently provides and/or directs the characterization of process optimization strategies and/or troubleshooting of operational issues in the operations, manufacturing, pilot plant or capital projects environment.

• Scope: Assembly, Tester and Packaging processes and machines support;
• Validation and Characterization experience (Protocols/URS/DS/IOQ/PQ); 
• Technical Report writing skills; 
• Basic knowledge and experience on
  Medical Device/Combo Product processes and regulations;
  metrology and testing experience; 
  project management skills
• Experience in medical device assembly process
• Statistical knowledge
• Machine troubleshooting
• Automation knowledge (PLC, HMI, Drivers, Motors, Profibus, Device Net, Control Net)

• Doctorate or Master’s degree in Engineering and 3 years of Engineering experience or 
• Bachelor’s degree in Engineering and 5 years of Engineering experience

• It is an Administrative shift, however there will be events that requires second and third shift support. Must be able to work in any shift as required by the projects and activities.