Analista De Automação - Divisão De Farmacêuticos Estabelecidos/manufatura (epd-m) - Rio De Janeiro/rj

Abbott

Rio de Janeiro, Rio de Janeiro, Brazil
Clp experience
Scada systems
Gmp compliance
Act as a key contributor to maintaining and improving industrial automation systems for pharmaceutical production

Job Summary

  • Act as a key contributor to maintaining and improving industrial automation systems for pharmaceutical production.
  • Ensure compliance with GMP, GAMP 5, and regulatory standards in a global healthcare company.
  • Work in a flexible, diverse, and innovative environment with opportunities for career growth.

Matching Summary

Act as a key contributor to maintaining and improving industrial automation systems for pharmaceutical production.

Skills & Requirements

Must-have

  • CLP experience
  • SCADA systems
  • GMP compliance
  • Industrial networks
  • Technical documentation
  • Root cause analysis

Nice-to-have

  • Pharmaceutical industry experience
  • MES integration
  • Cibersecurity knowledge

Key Requirements

  • Bachelor's degree in Electrical Engineering, Automation, or IT
  • Experience with CLPs (Siemens, Rockwell, Schneider, Omron)
  • Knowledge of industrial networks (Profibus, Ethernet/IP, Modbus)
  • 5+ years of experience in industrial automation

Work Rights

Not specified

Tailored Resume

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