Senior Expert Consultant – 14606

Publiceringsdatum: 2025-12-04

Är du intresserad av att jobba inom data/it? En möjlighet har öppnat upp för dig att börja arbeta som projektledare, it hos Veritaz AB. Om du vill arbeta heltid hos Veritaz AB, har de just nu en tjänst 6 månader eller längre som kan passa dig.

Platsen där jobbet finns ledigt är i ospecificerad arbetsort. Veritaz AB behöver fler anställda som stödjer arbetet inom projektledare, it. Kolla in deras lediga tjänst för att se om du har vad som krävs. Har du vad som krävs för att arbeta som projektledare, it hos Veritaz AB? Ansök innan lördag den tredje januari 2026 och ta reda på det!

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 Expert Consultant to join our dynamic team.

What you will work on

• Contribute expert knowledge to the national follow-up of the action plan for tissue donation and transplantation
• Lead work in collaboration with investigators and relevant stakeholders to drive initiatives connected to the action plan
• Develop, establish and implement new projects linked to prioritized measures
• Plan, coordinate and execute project activities, ensuring progress, quality and clear documentation
• Support regulatory-related work in the tissue area, including tasks connected to the Human Materials Regulation and adaptation to new requirements
• Contribute to additional assignments within tissue donation and transplantation where your professional expertise adds value
• Collaborate across organizational boundaries to strengthen national processes, harmonization and knowledge development in the field

What you bring

• Expert knowledge and proven experience within tissue donation, transplantation or adjacent medical/regulatory areas
• Strong ability to lead, plan and implement complex projects with multiple stakeholders
• Experience working with national strategies, action plans or regulated healthcare domains
• Good understanding of regulatory frameworks such as the Human Materials Regulation and their implications for healthcare operations
• Strong analytical and structured working style with the ability to translate complex issues into clear recommendations
• Excellent collaboration and communication skills, with the ability to work effectively with investigators, authorities and clinical partners
• A proactive, solution-oriented and responsible approach, with the ability to independently drive work forward while ensuring high quality
• Fluent in English and Swedish.