Statistics show that women and underrepresented groups tend to apply to jobs only if they meet 100% of the qualifications. Sobi encourages you to change that statistic and apply. Rarely do candidates meet 100% of the qualifications. We look forward to your application!

At Sobi, the work we do every day redefines the standards of care and transform the lives of people living with rare diseases.

As a diverse team of entrepreneurial people, we are passionate about our growth journey towards becoming a global leader, making a difference for rare disease patients, moving quickly and always challenging the status quo.

We are committed to an inclusive, sustainable and flexible workplace that fosters growth and development.

We are now searching for a Veeva Development Cloud Manager to join our IS/IT team. The IS/IT department is managed in-house and act as a strategic enabler for the implementation as well as the support and maintenance of business systems at Sobi.

As a Veeva Development Cloud Manager, you will be part of the Veeva Development Team within the Information System organization. The team supports Sobi’s quality systems i.e., the Veeva systems for Regulatory, Quality, Clinical Operation and Clinical Data. You will be system administrator in the Veeva Quality and Regulatory systems. The position has high visibility across the company and interacts globally with many departments as well as with external partners.

Sobi is a dynamic and growing company with a high pace of change. This requires well-functioning and up to date IT and business systems to support Sobi’s business strategies, and to ensure that we are fulfilling regulatory requirements applicable for the pharmaceutical industry.

Your main areas of responsibility will be the work with our Veeva Quality and Regulatory systems. You will act as system administrator and participate and lead new development projects and take care of day-to-day system maintenance and enhancements. You will work together with the rest of the team to handle the regular system updates in form of releases and act as a centre of competence for the Veeva GxP systems. This is a hands-on role combining system administration, configuration, solution design, and system evolution within the Veeva Development Cloud ecosystem.

The position is part of a Swedish team, with flexibility for remote work within the European time zone, reporting to the Head of Veeva Development based in Stockholm.

Examples of projects/areas to lead and support include:

• Act as the global System Administrator for the Veeva vault Quality and RIM
• Ownership of user access and account management
• Driving evaluation and adoption of system improvements in partnership with business stakeholders
• Leading system configuration and development activities, from planning through implementation
• Serving as System SME in development initiatives and cross‑functional projects
• Oversight of configuration impact assessments and release management
• Accountability for compliance documentation and ongoing regulatory alignment
• Representation in internal and external system forums
• Managing escalations to service providers and overseeing second‑line support
• Strategic collaboration with the other system managers in the team, system owners, IS/IT, and internal and external partners
• Monitoring and interpreting regulatory requirements related to computer compliance
• Leading and contributing to projects and validation activities

About you

You bring a strong background in quality and/or regulatory fields, with a natural interest in system development. You are an experienced, solution-oriented professional who enjoys taking ownership of complex tasks and enhancing how technology supports business strategy. You combine technical depth with a collaborative mindset and are comfortable operating in a global, regulated environment. You are curious, proactive, and your collaborative spirit and ability to manage and drive change will make you a vital part of our team.

• Experience of working with GxP systems as a Veeva system administrator.
• Strong problem-solving capabilities and ability to convert complex business requirements into robust system solutions.
• Knowledge of Quality and/or Regulatory applications and processes is a plus, as well as knowledge in document management systems.
• University Education in Computer Science or similar knowledge.
• Excellent communication skills in English is a must.
• Experience from the Pharmaceutical Industry will be considered a plus.

How to apply

We have an ongoing selection process in this recruitment and ask you to send your application as soon as possible. Click apply and include your resume in English. 

Why Join Us?

Here at Sobi, our mission and culture get us excited to come to work every day, but here are a few more reasons to join our team:

• Emphasis on work/life balance
• Collaborative and team-oriented environment
• Opportunities for professional growth
• Diversity and Inclusion
• Competitive compensation for your work
• Making a positive impact to help ultra-rare disease patients who are in need of life saving treatments

We are a global company with over 1,900 employees in more than 30 countries and are committed to the societies where we operate. With a deeply skilled management team directing our day-to-day wins, and a Board with a stellar track record, we’re ready to take on the world’s diseases, ailments and adversity. Our people believe they have the power to make a positive impact in others’ lives because that’s exactly what we do here. If you’re seeking a career that taps into your talents in a way that makes the world a better, healthier place, we just may have a job for you.

We know our employees are our most valuable asset, and our culture conveys that. We offer a competitive benefits package, to support the health and happiness of our staff.

Sobi Culture

At Sobi, we refuse to accept the status quo. This is because we have witnessed first-hand the challenges facing those affected by rare diseases and have used this knowledge to shape our business to find new ways of helping them.

As a specialized biopharmaceutical company, we are dedicated to rare diseases. And we see this focus as a strength. By effectively turning our research into ground-breaking treatments, we help make medicine more accessible and open up more possibilities for patients and more opportunities for those caring for them. This has been our approach since day one, but we know we can’t change the world of rare diseases on our own. Accomplishing this requires strong partnerships with patients, partners and stakeholders across the entire value chain. Together, we define how our business can create solutions that serve the needs of those affected by rare diseases while facilitating sustainable growth.