Senior Quality Applications Specialist

Are you passionate about driving excellence in regulated environments and shaping the future of quality systems? Join a well-established life sciences organization focused on developing and delivering innovative cell-based therapies that improve patient outcomes worldwide.

• Act as the expert for global Quality applications (e.g., Veeva Quality Docs, Veeva QMS, LIMS), ensuring they remain compliant, user-friendly, and fit for purpose.
• Manage the full application lifecycle, including configuration, access management, documentation, validation readiness, and performance monitoring in a GxP-regulated environment.
• Collect and analyse business requirements from global and local stakeholders, translating them into clear solution designs and change requests.
• Coordinate system changes and releases, including design, testing, validation documentation, and user acceptance.
• Serve as the escalation point for functional support, incidents, and problem resolution, collaborating with internal IT teams and external vendors.
• Drive continuous improvement and digitalisation, using insights, user feedback, and industry best practices.
• Build and maintain a global network of key users and site administrators, including training, roadmap communication, and release updates.

• Bachelor’s degree in IT, Business Informatics, Life Sciences, or a related field.
• 5–7 years’ hands‑on experience with Quality applications in the pharmaceutical or life‑science industry.
• Strong practical experience with systems like Veeva Quality Docs, Veeva QMS, LIMS, or other regulated platforms.
• Solid understanding of GxP requirements, validation principles, and regulated system environments.
• Proven experience in requirements management, change coordination, testing, and validation.
• Strong analytical, conceptual, and problem‑solving skills, with excellent stakeholder management.
• Fluency in English

Be part of a team that drives compliant, efficient, and innovative Quality processes on a global scale.