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); 

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.

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

• Administrative/Non-Standard shift