Sr Engineer – Software # JN -072021-66950

*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.