Sr Engineer – Software # JN -072021-66950

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Industry: Database Administrator / Engineers
Job Number:

*Onsite role-local candidates who can start immediately are needed.

***Must have Pharmaceutical, Biotech, Medical Device, FDA industry experience with cGMP regulations

 

Description:

The Automation Engineer will:

  • Provide hands-on PLC/DCS/BMS/HMI/SCADA programming services including
  • development work for integration of new systems and upgrade of existing systems.
  • Support and review validation documents.
  • Provide Project Engineering support for the automation project cycle on large project.
  • Provide direct hands on experience with lifecycle management of control systems hardware and software infrastructure.

 

 

Basic Qualifications:

  • Doctorate Degree

OR

  • Master's Degree and 3 years of Engineering experience

OR

  • Bachelor's Degree and 5 years of Engineering experience

OR

  • Associate's degree and 10 years of Engineering experience

OR

  • High school diploma/GED and 12 years of Engineering experience

 

 

Preferred Qualifications

  • Bachelor’s in electrical, chemical, or mechanical engineering or Advanced degree.
  • Min. 5+ years of experience in troubleshooting and designing of DeltaV DCS systems.
  • Min. 7+ years of experience working on Rockwell Automation and Allen-Bradley PLCs (Factory Talk & ControlLogix), and/or ABB DCS.
  • Project engineering skills over and above the technical skills.
  • Excellent people, team, and verbal/written communication skills.
  • Experienced in process control engineering.
  • Experience with Process Design, Commissioning and change control methodology.
  • Direct experience with regulated environments including detailed understanding of cGMPs.
  • Ability to update and read P&IDs, instrumentation and electrical design packages including SDS, HDS, URS, IQ, OQ, VP and VSR among other engineering and validation documentation. Develop of detailed specification, engineering documents, SOP and operating standards.
  • Able to support manufacturing operations through effective troubleshooting and ensuring automated equipment uptime and reliability.
  • Knowledge of OSI PI Historian.
  • Pharmaceutical, Biotech, Medical Device, FDA industry experience with cGMP regulations.
  • Ability to work with others in a team environment
  • Strong focus on safety.
  • Some documentation and computer system validation experience.
  • Automation / Controls engineering experience in a system integrator environment.
  • Direct hands on experience with lifecycle management of control systems hardware and software infrastructure.


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