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

Log on now to our website http://www.qrcgroup.com/ to learn more about our services and solutions!

Sr Associate Manufacturing Systems with working knowledge of pharmaceutical/biotech processes. Background in programming, installation of manufacturing process controls, automation and field instrumentation technologies. Familiarity with validation processes and documentation in a highly regulated environment.

Skills in the following areas: 

• Rockwell Automation Platform and Allen-Bradley PLCs
• Rockwell Automation Factory Talk & ControlLogix PLC Platform
• Rockwell SLC500 PLC families Controllers
• Rockwell Automation FTView SE and FTBatch systems
• DeviceNet technologies
• Programming language (e.g. VBA, SQL) 
• Serialization process
• Knowledge in robot or robot programming
• Knowledge in vision system technology
• Problem solving and root cause analysis 
• Technical report writing
• Technical presentations

Work schedule flexibility to support 24/7 operations (shift: 5:00 am to 5:30 pm or 5:00pm to 5:00 am included alternate weekend)

• Master’s degree or Bachelor’s degree and 2 years of Engineering experience or Associate’s degree and 6 years of Engineering experience 
• Bilingual (English/Spanish) (Written/Speak)
• Personal Organization
• Dealing with and managing change
• Analytical Problem Solving
• ​Computer Literacy

Work schedule flexibility to support 24/7 operations (shift: 5:00 am to 5:30 pm or 5:00pm to 5:00 am included alternate weekend)

All your information will be kept confidential according to EEO guidelines.