Senior IT Specialist – 13521

Publiceringsdatum: 2025-10-07

Funderar du på att söka jobb inom data/it? En möjlighet har öppnat upp för dig att börja arbeta som projektledare, it hos Veritaz AB. Vill du arbeta heltid hos Veritaz AB? Just nu letar de efter någon som vill ha en tjänst 6 månader eller längre.

För detta jobb är det en fördel om du bor i närheten av ospecificerad arbetsort då det är tjänsteorten. Om du letar efter en spännande karriär inom projektledare, it-branschen, har Veritaz AB just nu ett ledigt jobb som kan vara av intresse. Söker du efter en spännande karriär som projektledare, it? Sök jobbet hos Veritaz AB senast torsdag den sjätte november 2025 och bli en del av deras team.

Jobbannons

Veritaz is a leading IT staffing solutions provider in Sweden, committed to advancing individual careers and aiding employers in securing 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 a Senior IT Specialist to join our dynamic team.

What you will work on

• Develop, manage, and maintain the IT infrastructure for the Chemical Processes and Pharmaceuticals department
• Provide daily IT support and troubleshooting for computerized systems
• Plan maintenance, upgrades, and further development of systems to ensure operational efficiency and compliance
• Support the purchase, implementation, and validation of new instruments and systems, ensuring adherence to regulatory requirements
• Train colleagues on IT-related systems and procedures
• Act as IT representative during inspections, explaining compliance with regulatory and GMP requirements
• Collaborate with the technical team and contribute to other system-related tasks as needed

What you bring

• Strong analytical and problem-solving skills with a structured and efficient approach
• Experience acting as an IT representative during regulatory or customer inspections
• Knowledge of laboratory instrument data handling, including data storage, traceability (audit trails), and data integrity principles
• Excellent communication skills in Swedish and English, both written and verbal
• Experience working in and administering SharePoint
• Solid understanding of IT environments, including Windows OS, network structures, directory services (AD/LDAP), and basic scripting
• Documented GMP experience from an IT perspective, including qualification documentation and handling deviations linked to IT systems
• Advantageous: previous experience in pharmaceutical or other regulated industries