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

Lorven Technologies Inc
Piscataway, NJ, United States
18 days ago
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Role details

Contract type
Permanent contract
Employment type
Full-time (> 32 hours)
Experience level
Expert
Experience required
5 years minimum
Working hours
Regular working hours
Job source

Tech stack

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
+1 more
GXP

Requirements

  • 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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