The Small-Scale Organics (SSO) Pilot Plant is a Good Manufacturing Practices (GMP) facility which enables gain of critical internal experience during scale-up of clinical supplies manufacturing, demonstration of new manufacturing technology/processes, training opportunities for improved manufacturing process development, and seamless technology transfer to commercial sites.
This Dela V SSO Automation Engineer role within the SSO Pilot Plant leverages scientific, technical, and operational experience to support facility operations, process development activities, compliance investigations and change management processes. The position is responsible for implementing automation changes that meet Safety and Environment (S&E) and GMP requirements as well as ensuring facility readiness for a highly manual batch process. In addition, this position is expected to work cooperatively with the SSO partners to drive overall success of the pilot plant. The Automation Engineer is required to be on-site fulltime and reports to a Senior Automation Engineering leader. You will help deliver IT and automation solutions to the SSO Pilot Plant. This encompasses a wide range of manufacturing technology, primarily DeltaV, also includes AB PLCs, historians, and supporting IT applications, all aligned to a goal of ensuring frictionless flow of data and more efficient business operations. You will be able to make an impact by participating in troubleshooting and root-cause analysis to ensure that our automation systems operate with minimal downtime.
This role is on-site 5 days a week and requires occasional off hours work to handle emergencies.
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B.S. degree in Electrical Engineering / Chem E or Comp. Sc., or relevant technical field.
Min. 2 years of Industrial Automation experience with HMI, SCADA, DCS Delta V, PLC, I & C etc.
Min. 2 year of hands-on Delta V systems experience.
Some experience with regulated Manufacturing process Industry
Experience with automation system architecture, design, start-up, and/or qualification.
Experience working in GAMP regulated environment (prefeerably pharma)
BioPharma GMP manufacturing experience.
Experience working with MS SQL Server or Oracle database.
Experience with batch, CIP, SIP processing.
Delta V training or certification from Emerson
Experience with control system validation.
Some Project Engineering or Maintenance experience
Benefit packages for this role will start on the 31st day of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA account options, and 401k retirement account access with employer matching. Employees in this role are also entitled to paid sick leave and/or other paid time off as provided by applicable law.