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GMP Automation Engineer 18581

Fast + rörlig lön Tidsbegränsad anställning

Veritaz AB · — · Org.nr verifierat · publicerad 16 jul 2026 · sista ansökningsdag 15 aug 2026

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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