Manufacturing Execution System (mes) -lead

J&J FAMILY OF COMPANIES

Wilson, North Carolina, United States
Not specified
Mes platform expertise (werum pas-x)
Integration with it and dcs systems
Project management of mes configuration
Johnson & Johnson is seeking a Manufacturing Execution System (MES) Lead for their new facility in Wilson, North Carolina, aimed at expanding their capacity for producing innovative biologic medicines. The ideal candidate will have extensive experience in the biopharmaceutical industry and expertise in MES platforms, as well as strong leadership and problem-solving skills

Job Summary

  • Johnson & Johnson is expanding manufacturing capacity with a $2 billion investment to support portfolio growth and deliver breakthrough biologic medicines.
  • The MES Lead will drive design, deployment, and continuous improvement of the site MES system, collaborating cross-functionally and managing vendors to ensure system requirements are met.
  • The role supports a highly automated production process with real-time data sharing across platforms to enhance productivity and data accuracy.

Matching Summary

Match Score: 85

Johnson & Johnson is seeking a Manufacturing Execution System (MES) Lead for their new facility in Wilson, North Carolina, aimed at expanding their capacity for producing innovative biologic medicines. The ideal candidate will have extensive experience in the biopharmaceutical industry and expertise in MES platforms, as well as strong leadership and problem-solving skills.

Skills & Requirements

Must-have

  • MES platform expertise (Werum PAS-X)
  • Integration with IT and DCS systems
  • Project management of MES configuration
  • Technical leadership of vendor teams
  • GMP regulated manufacturing environment
  • Computer System Validation (CSV)
  • Cross-functional collaboration

Nice-to-have

  • Industry 4.0/IoT appreciation
  • Experience with DeltaV PAS & OSI PI integration
  • Batch release report knowledge
  • Strong programming skills (.NET, SQL, PL/SQL, Java)
  • Analytical and problem-solving skills
  • Mentoring junior engineers

Key Requirements

  • Bachelor’s degree in engineering, IT, or related field
  • Minimum 8 years manufacturing or pharmaceutical experience
  • Knowledge of cGMP regulations including 21 CFR Part 11 and EU GMP Annex 11
  • Experience in supervision and resource management
  • Ability to travel up to 10%
  • Experience in pharmaceutical GMP manufacturing environment

Work Rights

Not specified

Tailored Resume

Cover Letter