GMP Automation Engineer 18581

Publiceringsdatum: 2026-07-16

Letar du efter anställning inom yrken med teknisk inriktning? Positionen som automationsingenjör, maskin hos Veritaz AB är öppen och väntar på en lämplig kandidat - kan det vara du? Intresserade sökes för heltid-jobb hos Veritaz AB - är du intresserad? De letar efter någon som vill jobba 6 månader – upp till 12 månader.

För detta jobb är det en fördel om du bor i närheten av ospecificerad arbetsort då det är tjänsteorten. Veritaz AB har just nu en ledig tjänst som automationsingenjör, maskin. Om du vill ta din karriär till nästa nivå, ta en titt på deras jobbannons och se om jobbet passar dig! Du har fortfarande tid att söka jobbet som automationsingenjör, maskin hos Veritaz AB om du sickar in din ansökan senast sista ansökningsdag som är lördag den femtonde augusti 2026.

---

Jobbannons

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