
Veritaz AB · Sweden
Som GMP Automation Engineer kommer du att konfigurera och optimera styrsystem samt integrera processutrustning inom hårt reglerade miljöer.
Som GMP Automation Engineer kommer du att konfigurera och optimera styrsystem samt integrera processutrustning inom hårt reglerade miljöer.
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
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 Process Engineer What You Will Work On Translate process requirements into practical manufacturing solutions Develop process descriptions, process parameters, operating limits, and process documentation Support process development for GMP manufacturing operations Develop and optimize batch processes and recipe management Work with DeltaV or equivalent automation platforms Define process parameters, setpoints, and operating boundaries Support commissioning, process verification, testing, and startup activities Troubleshoot process and production issues Collaborate closely with automation, validation, and commissioning teams Support process safety through alarm philosophy and interlock design Ensure compliance with GMP/GxP standards and regulatory requirements Participate in process optimization and continuous improvement initiatives Prepare and maintain technical documentation throughout the project lifecycle What You Bring Experience as a Process Engineer within the pharmaceutical, biotech, or other GMP/GxP-regulated industries Strong understanding of batch manufacturing processes and recipe development Experience with DeltaV or similar Distributed Control Systems (DCS) Experience defining process parameters, setpoints, and operating limits Understanding of alarm philosophy, interlocks, and process safety principles Experience with process verification, testing, commissioning, and troubleshooting Experience collaborating with automation and validation teams Strong technical documentation skills Experience working in highly regulated manufacturing environments Good communication and collaboration skills
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 Lead What You Will Work On Lead the overall automation workstream for a major pharmaceutical investment project Define and drive the automation strategy and control philosophy Lead automation system design, implementation, testing, and deployment Design and implement DeltaV automation architecture and solutions Develop and manage batch automation systems and recipe implementation Coordinate system integration between equipment, automation platforms, and surrounding systems Design and review sequence logic, interlocks, alarm management, HMI solutions, and operator interfaces Lead technical design reviews and make key technical decisions Coordinate automation engineers and cross-functional technical teams Collaborate closely with process, validation, commissioning, and production teams Plan and oversee FAT, SAT, automation testing, and verification activities Ensure compliance with GMP, GxP, and Computerized System Validation (CSV) requirements Support commissioning, qualification, and operational readiness of automation systems Prepare and maintain automation documentation, functional specifications, and control strategies What You Bring Several years of experience leading automation projects within the pharmaceutical industry or other GMP/GxP-regulated environments Deep expertise in process automation, batch systems, and control strategies Extensive hands-on experience with DeltaV architecture, design, and implementation Strong experience with batch control, recipe implementation, and system integration Solid understanding of sequence logic, interlocks, alarm management, HMI design, and operator interfaces Experience integrating equipment with automation and surrounding systems Strong knowledge of GMP, GxP, and Computerized System Validation (CSV) Experience leading technical design reviews and making architecture decisions Proven ability to lead automation engineers and coordinate cross-functional technical teams Experience planning and executing FAT, SAT, automation testing, and verification Excellent leadership, communication, and stakeholder management skills
Multiply is building a strong pool of senior automation professionals for current and upcoming assignments within advanced manufacturing, robotics, automotive, energy, process industry, Life Sciences and industrial digitalisation. Your role Depending on your background, you may: Lead automation activities from design to commissioning and production support Develop and modify PLC, HMI, SCADA and DCS systems Take technical ownership of machines, production lines, process equipment or robot cells Troubleshoot production-critical systems and lead root-cause analysis Modernise existing automation platforms Coordinate suppliers and multidisciplinary engineering teams Support machine safety, functional safety and OT/IT integration Plan and coordinate automation work packages, milestones, risks, dependencies and technical deliverables Support customer communication, progress reporting and technical decision-making You may work in both project and production environments. This can include daily production support, troubleshooting and root-cause analysis, preventive improvements, equipment modifications, FAT/SAT, commissioning and production ramp-up. Experience with electrical drawings, control cabinets, industrial maintenance and production-critical systems is highly valuable. Your profile You have solid experience in industrial automation and specialist competence in one or more of the following areas: PLC engineering: Siemens S7 and TIA Portal, Allen-Bradley and Rockwell Automation, Beckhoff TwinCAT, Schneider Electric, Mitsubishi, Omron or similar platforms ABB automation: ABB 800xA, AC 800M, System 800xA, ABB robotics or related control environments HMI and SCADA: WinCC, FactoryTalk, AVEVA System Platform, Ignition or comparable supervisory systems Process automation and DCS: PCS 7, ABB 800xA, instrumentation, batch control and process-control systems Industrial robotics: ABB, KUKA, FANUC or similar platforms, including programming, cell integration and commissioning Motion and drives: Servo systems, frequency converters and coordinated machine control Industrial communication: PROFINET, PROFIBUS, EtherCAT, Modbus TCP, OPC UA or industrial Ethernet Machine safety: Safety PLCs, functional safety, machinery regulations and CE-related engineering OT/IT integration: MES, databases, APIs, production-data platforms, industrial middleware and cybersecurity Testing and commissioning: FAT, SAT, virtual commissioning, production ramp-up and troubleshooting Brownfield modernisation: Upgrades, migrations and modifications to production-critical systems Life Sciences automation: GMP-regulated production, validation, traceability, structured documentation and controlled system changes Experience in project management, technical project leadership or work-package coordination is meriting. This may include planning, estimation, risk management, supplier coordination, stakeholder communication, progress reporting and responsibility for scope, schedule and technical deliverables. Experience with GAMP 5, computerised-system validation, qualification activities, audit trails, electronic records, batch systems or regulated change control is also meriting for Life Sciences assignments. You do not need experience in every area. We are particularly interested in candidates with recognised depth in at least one automation domain and the ability to understand how machines, control systems, data, networks and production processes interact. You are comfortable combining hands-on engineering with technical responsibility, customer dialogue and coordination across engineering disciplines. You communicate confidently in English. Swedish is meriting, particularly for production-facing and customer-site assignments. Work with VisFlow Operational World At Multiply, automation is connected with industrial data, systems engineering, cybersecurity and operational improvement through our VisFlow platform. VisFlow Operational World is an offering within our VisFlow platform where we are building a live, connected representation of an enterprise's operations. It brings together machines, production systems, applications, data flows, networks, assets and business processes into a single operational model. This enables real-time visibility, dependency analysis, operational insights and intelligent automation across the enterprise. As a senior automation professional, your domain expertise can help connect production-floor systems with the wider operational environment and support smarter, more resilient and better-coordinated operations. Why Multiply? At Multiply, you can: Work in advanced Swedish industrial environments Combine technical leadership with hands-on engineering Influence architectures, standards and delivery methods Contribute to VisFlow and industrial digitalisation Help shape Multiply's growing automation offering Apply Apply through the Multiply careers portal on our website. We review applications continuously.