Sr Engineer – Software # JN -072021-66950
,
Posted on: July 13, 2021
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.