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# Manufacturing Systems Engineer SCADA / MES / Track & Trace (Pharma)

- **Company:** Lorven Technologies Inc
- **Location:** Piscataway, NJ, United States
- **Experience:** Expert
- **Contract:** Permanent contract
- **Skills:** Communications Protocols, Data Integrity, Serialization, Supervisory Control and Data Acquisition (SCADA), Wonderware, SAP (Applications), Data Streaming, System Testing, Systems Integration, Information Technology, Syncade, Allen-Bradley Factory Automation Equipment, GXP
- **Published:** August 18, 2026
- **Apply:** https://www.dice.com/job-detail/0f0c3582-5d52-497d-ac88-922eadf43436

## About the Role

* Bachelor's degree in Engineering, Computer Science, or related field.
 * Must have a 5+ years of experience in pharmaceutical or regulated manufacturing environments.
 * You should have a Hands-on experience with SCADA systems (e.g., Wonderware, Ignition, Siemens WinCC, FactoryTalk).
 * Must have a Strong experience with MES platforms (e.g., Werum PAS-X, Syncade, Camstar, Opcenter).
 * You should have Proven experience in Track & Trace / Serialization systems (e.g., TraceLink, Systech, Antares Vision, Optel).
 * Good Knowledge of packaging line integration including serialization equipment and aggregation
 * You should have a Good Understanding of DSCSA requirements and global serialization regulations.
 * Must have an Experience with PLC systems (Allen-Bradley, Siemens) and industrial communication protocols.
 * You should have a Familiarity with SAP integration (PP/MM) and data flow between systems.
 * Strong Experience with validation and regulatory compliance (GxP, 21 CFR Part 11).
 * Good Experience in Data integrity and system validation
 * You should have Cross-system integration (PLC-MES-ERP-Serialization)
 * Good Experience in solid oral dose (OSD) manufacturing and packaging operations.
 * You should have a Exposure to vision inspection systems and labeling/printing technologies.
 * Good Knowledge of IIoT, digital manufacturing, or Industry 4.0 initiatives.
 * You should have a Good Experience working in FDA-inspected facilities.
 * Strong documentation and cross-functional communication skills.



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