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Ny GMP Automation Engineer 18581
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Ansökt Ångra
Publicerad idag
Ansökt Ångra
Ingenjör Automationsingenjör
Publicerad idag

Arbetsbeskrivning

Veritaz is a leading IT staffing solutions provider in Sweden, committed to advancing individual careers and aiding employers in ensuring the perfect talent fit. With a proven track record of successful partnerships with top companies, we have rapidly grown our presence in the USA, Europe, and Sweden as a dependable and trusted resource within the IT industry.

Assignment Description

We are looking for an experienced Automation Engineer

What You Will Work On

  • Develop and configure automation solutions for pharmaceutical manufacturing systems
  • Design and implement control logic, sequences, phases, and interlocks
  • Configure and optimize DeltaV or equivalent DCS automation platforms
  • Develop HMI screens and operator interface solutions
  • Configure alarm management and control strategies
  • Integrate process equipment with control systems and higher-level applications
  • Support batch control and recipe implementation
  • Participate in FAT, SAT, commissioning, and system verification activities
  • Troubleshoot automation systems during testing and startup
  • Prepare and maintain automation documentation and technical specifications
  • Support qualification and Computerized System Validation (CSV) activities
  • Collaborate with process, validation, commissioning, and engineering teams
  • Ensure compliance with GMP, GxP, and pharmaceutical quality standards
  • Support system improvements and automation optimization throughout the project lifecycle

What You Bring

  • Experience as an Automation Engineer within the pharmaceutical industry or another GMP/GxP-regulated environment
  • Strong hands-on experience with DeltaV or similar DCS/process automation platforms
  • Experience configuring control logic, sequences, phases, interlocks, and alarm functions
  • Experience developing HMI applications and operator interfaces
  • Experience integrating process equipment with automation and supervisory systems
  • Good understanding of GMP, GxP, and Computerized System Validation (CSV)
  • Experience performing FAT, SAT, commissioning, startup, and automation verification
  • Experience troubleshooting, testing, and documenting automation solutions in regulated environments
  • Ability to work effectively with process, validation, and commissioning teams
  • Strong analytical, troubleshooting, and communication skills


Mer info

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Publicerad 2026-07-16
Antal platser 1
Hemsida Länk
Dela annons

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