AbbVie, Branchburg, NJ, Onsite
About AbbVie
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at [www.abbvie.com](http://www.abbvie.com/). Follow @abbvie on [LinkedIn,](https://www.linkedin.com/company/abbvie/) [Facebook](https://www.facebook.com/AbbVieGlobal/), [Instagram](https://www.instagram.com/abbvie/), [X](https://twitter.com/abbvie) and [YouTube.](https://www.youtube.com/user/AbbVie)
Responsible for the design, implementation, integration and maintain automation systems across manufacturing operations. Responsible for moderate to complex configuration and programming of Operation Technology (OT) Systems as per AbbVie change management procedures for the manufacturing process, utilities and Facilities Control Systems. This role is responsible for leading small to medium-sized automation projects to assure project is implemented as per project schedule. This role provides technical support and system troubleshooting for systems and/or areas assigned to this position. Responsible for the administration and maintenance of assigned OT systems as per applicable departmental procedures.
Responsibilities
Bachelor’s degree in Computer Science, Engineering, or related discipline with a minimum of six (6) years of relevant experience required. Master’s degree in Computer Science, Engineering, or related discipline with a minimum of four (4) years of relevant experience.
Working experience administering and/or configuring of Distributed Control Systems (DCS) such as Emerson DeltaV, Foxboro I/A.
Working experience with SCADA and PLCs (such as Allen-Bradley ControlLogix), programming in ladder logic and instructional texts.
Experience with commissioning and qualification activities, including computerized systems validation.
Solid understanding of pharmaceutical and biotechnology manufacturing processes, including operational best practices and regulatory expectations.
Industry experience exposure to FDA , GMP , 21CFR11 , Data Integrity, Safety and Environmental legislation.
Preferred:Bachelor’s degree in Engineering is Highly Desired
(6) years of experience with Automation Equipment specifically in SCADA and PLC programming in ladder logic and instructional texts is Highly Desired
Experience with HMI graphics development and management is Desired
Experience administering and/or configuring a data historian system is Desired