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Form of workJob Description
About Client:
Our client is growing its locations and is investing more than $2 billion into establishing a new large-scale manufacturing site for biopharmaceuticals in the United States to accelerate the growth of their Bio CDMO (Contract and Development Manufacturing Organization) business. The new site will offer end-to-end solutions to their customers looking to manufacture biopharmaceuticals in the US. The new site is to be located in Holly Springs, North Carolina.
We are searching for a highly motivated DeltaV Process Automation Engineer who wants to participate in our journey to establish the largest end-to-end cell culture CDMO facility in North America. In the project phase, your main responsibility will be to provide Engineering input on the design and implementation of an Emerson DeltaV control system in the area of Buffer Preparation/Hold, Purification – Chromatography (LPC), Viral Filtration (VF), Ultrafiltration (UF), Diafiltration (DF), and Dispensing. Once in Operations, you will be responsible for and have ownership of the ongoing support of the control system for the defined process areas. You will report to the Automation Lead for DSM.
Responsibilities:
- Support the design and implementation of a DeltaV control system for the automation of a CDMO facility.
- Ensure project implementation is well received throughout the organization.
- Coordinate with vendors as it relates to the Emerson DeltaV control system
- Interface with the IT/OT and I&C teams for coordination and integration of the control system.
- Manage hardware/software design decisions and change control in a regulated environment.
- Opportunities to make periodic International and Domestic travel.
- You should expect the role and responsibilities to develop and evolve as the project group expands.
Requirements:
- Bachelor’s degree in Chemical Engineering, Electrical Engineering, Computer Science, Biological Science, or equivalent.
- 5+ years of experience designing, configuring and implementing Emerson DeltaV control systems for Downstream operations using ISA-88 standards.
- Excellent oral and written communications skills and fluency in English.
- Collaborative attitude with the willingness to work with global peers and cross-functional teams toward the company and department goals.
- Experience in a cGMP facility or working with FDA regulations.
- Knowledge of Drug Substance Manufacturing (DSM) would be beneficial.
- Knowledge of Emerson Syncade, OSIsoft PI, InfoBatch, and Siemens PLCs is a plus.
