[Hiring] Veeva Development Cloud Manager @Sobi

Role Description

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 acts 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 the 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.

Your main areas of responsibility will include:

• Acting 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 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

Qualifications

• Strong background in quality and/or regulatory fields
• 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
• 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

Benefits

• 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