Sida 1 av 1
Sökrapport & Insikter
Dina pendlingsinställningar är aktiverade, men eftersom Skåne ligger utanför ditt pendlingsavstånd visar vi alla 3 st lediga tjänster som matchar sökordet "CSV" i regionen, sorterade efter matchningspoäng (bäst restid och lön först).
Tips: Vill du bevaka denna sökning? för att skapa en gratis jobbspanare och få mejl om nya matchande tjänster! 🔔
Ej specificerad•Heltid•Publicerad: 16 juli•Sista ansökan: 15 aug.
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
DeltaVGMPAutomation Manager
Stockholm•Heltid•Publicerad: 20 maj•Sista ansökan: 17 nov.
Vi söker valideringsingenjörer till kommande uppdrag inom Life Science i Stockholm och Uppsala. Efterfrågan på validering är hög, och vi vill nu komma i kontakt med dig som vill arbeta med kvalificering och validering i regulatoriskt styrda miljöer. Om rollen Du arbetar med validering och kvalificering av utrustning, processer eller datoriserade system. Exempel på arbetsuppgifter: Planering och genomförande av IQ/OQ/PQ Framtagning av valideringsdokumentation Riskanalyser och kravställning (URS) FAT/SAT, commissioning Säkerställa regelefterlevnad enligt GMP, GAMP5 Vi söker dig som: Har erfarenhet av validering inom Life Science Har arbetat med IQ/OQ/PQ och dokumentation Har god kunskap inom GMP Gärna har erfarenhet av CSV eller processvalidering Vi arbetar både med konsultuppdrag och rekryteringar och tar gärna en dialog kring dina preferenser. Urval sker löpande och eftersom detta är en proaktiv annons så återkopplar vi så snart som möjligt. Om verksamheten Du kommer att arbeta som konsult hos en av QRIOS partners inom Life Science, i en forskningsintensiv miljö där innovation och vetenskaplig excellens står i fokus. Teamet består av både juniora ingenjörer och seniora forskare som tillsammans driver projekt inom filtrering, rening och analytisk utveckling. Om QRIOS Life Science QRIOS är din pålitliga partner inom Life Science-sektorn. Vi är experter på rekrytering och konsultlösningar för specialist- och chefsroller inom läkemedel, medicinteknik, bioteknik, kemiteknik och livsmedelsteknik. Vår styrka ligger i att våra medarbetare själva har omfattande erfarenhet från branschen, vilket ger oss en unik förståelse för våra kunders behov och utmaningar. Som konsult hos QRIOS får du möjlighet att prova på olika uppdrag, utvecklas snabbt och bygga ett brett nätverk inom Life Science. Tillsammans driver vi innovation och bidrar till en bättre framtid.
ValideringsingenjörLife ScienceGMP
Ej specificerad•Heltid•Publicerad: 15 juli•Sista ansökan: 14 aug.
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 Validation Lead What You Will Work On Define and lead the overall validation strategy for the project Develop verification and qualification approaches for technical systems and equipment Lead validation activities across project phases Perform and coordinate risk assessments related to validation Ensure full compliance with GMP and GxP regulations Lead Computerized System Validation (CSV) activities Validate computerized systems, manufacturing processes, and technical equipment Support validation of DeltaV or similar automation platforms Develop and maintain traceability matrices Coordinate qualification activities including IQ, OQ, and related verification processes Manage validation documentation and compliance deliverables Lead deviation investigations, CAPA activities, and corrective actions Collaborate with automation, process, commissioning, engineering, and quality teams Coordinate validation activities across multiple stakeholders Ensure successful delivery of validation objectives within project timelines What You Bring Several years of validation experience within the pharmaceutical industry Strong knowledge of GMP and GxP regulatory requirements Extensive experience with Computerized System Validation (CSV) Experience validating computerized systems, manufacturing processes, and technical equipment Practical experience with DeltaV or similar automation platforms in regulated environments Experience developing validation strategies and verification approaches Experience conducting risk assessments and qualification planning Experience with traceability matrices and requirements management Experience handling deviations, CAPA, and validation documentation Strong leadership, coordination, and stakeholder management skills Excellent communication and technical documentation skills
Validation LeadComputer System ValidationGMP
Pendling
Restidsgräns45 min
🚀 15 min🇸🇪 45 min snitt🚌 90 min
Pendlingskarta (Skåne)
Optimal (< 25 min)
Standard (25-50 min)
Långp. (> 50 min)
Utanför gräns (> 45 min)