Manufacturing Execution System (mes) -lead

Johnson & Johnson Innovative Medicine

Wilson, North Carolina, United States
Hybrid
Mes platforms (e.g., werum pas-x)
Mes software platforms
Opc servers and clients
Johnson & Johnson Innovative Medicine is seeking a Manufacturing Execution System (MES) Lead to oversee the design and implementation of the Kroeber PAS-X MES at their new manufacturing facility in Wilson, North Carolina. The ideal candidate will have substantial experience in the pharmaceutical or biopharmaceutical industries, with strong technical and leadership skills to enhance productivity through digital solutions

Job Summary

  • The MES Lead drives the design and configuration activities of site’s Kroeber PAS-X MES, including MBR design, vendor management, production, validation and development systems, system standards, and interfaces to DCS & IT systems.
  • Collaborate cross-functionally with Manufacturing, Quality, Engineering, and IT to identify and implement digital solutions that enhance productivity and data accuracy.
  • Lead the planning, execution, and completion of MES application configuration activities like MBR, item management, equipment management, label management from start to finish.

Matching Summary

Match Score: 85

Johnson & Johnson Innovative Medicine is seeking a Manufacturing Execution System (MES) Lead to oversee the design and implementation of the Kroeber PAS-X MES at their new manufacturing facility in Wilson, North Carolina. The ideal candidate will have substantial experience in the pharmaceutical or biopharmaceutical industries, with strong technical and leadership skills to enhance productivity through digital solutions.

Skills & Requirements

Must-have

  • MES platforms (e.g., Werum PAS-X)
  • MES software platforms
  • OPC servers and clients
  • cGMP regulations related to CSV
  • 21 CFR Part 11 and EU GMP Annex 11
  • pharmaceutical or GMP regulated manufacturing environment

Nice-to-have

  • Industry 4.0/IoT appreciation
  • integrating MES with DeltaV PAS
  • OSI PI data historian integration
  • batch release reports
  • release by exception

Key Requirements

  • 8+ years in manufacturing, biopharmaceutical or pharmaceutical
  • Bachelor’s degree in engineering, IT, Science
  • Supervision/management of people and resources
  • Process knowledge for Upstream, Downstream and Bio Processing

Work Rights

Not specified

Tailored Resume

Cover Letter