Senior Veeva Configuration Specialist

<p><em>Are you passionate about&nbsp;the Veeva platform? Do you have experience&nbsp;from a configuration perspective&nbsp;and want to work hands-on with configuration?&nbsp;</em></p><p><em>If so, now is your chance to join Ascendis Pharma&nbsp;as our new Configuration Specialist for the Veeva platform&nbsp;</em></p><p></p><p><strong>Ascendis Pharma&nbsp;</strong>is a global biopharmaceutical company committed to making a meaningful difference in patients’ lives. Guided by our core values of Patients, Science, and Passion, we are applying our innovative TransCon® technology platform to fulfill our mission of developing new therapies that&nbsp;demonstrate&nbsp;best-in-class potential to address unmet medical needs.&nbsp;&nbsp;</p><p>At our headquarters in Hellerup, Denmark, research facilities in Heidelberg, Germany, and&nbsp;additional&nbsp;offices across Europe and the United States, we are advancing programs in our Endocrinology Rare Disease and Oncology portfolios. We also collaborate with partners on the development of TransCon-based products in other therapeutic areas and markets.&nbsp;&nbsp;</p><p></p><p><strong>We are seeking</strong>&nbsp;a passionate Configuration Specialist to join our growing team. As a key member of the Ascendis Pharma team, you will play a crucial role in&nbsp;supporting and&nbsp;enhancing&nbsp;our Veeva Systems (Quality &amp; Regulatory) and our platform landscape across regulated (GxP) domains.&nbsp;&nbsp;&nbsp;</p><p>This is an exciting opportunity to work in a fast-paced environment,&nbsp;collaborating&nbsp;with cross-functional, global teams working together to achieve extraordinary results.&nbsp;</p><p>You will be joining our Team&nbsp;Auhtority&nbsp;product team and report directly to&nbsp;Lene Rhein Larsen, People Leader in Global IT, and work closely with Product Owner, Maribel Estrada, on the functional side. You will be based in Hellerup.&nbsp;</p><p></p><p><strong>Your key responsibilities will be:</strong>&nbsp;</p><p>This role is hands-on and configuration-heavy, focused on designing, building, and&nbsp;maintaining&nbsp;scalable, compliant Veeva&nbsp;best practice&nbsp;solutions in close collaboration with Business, QA, and IT stakeholders.&nbsp;</p><ul><li>&nbsp;Design and implement object models, workflows,&nbsp;lifecycles,&nbsp;and much more.&nbsp;</li><li>Partner with Business and Validation to ensure compliant configurations.&nbsp;</li><li>Support release planning, regression testing, and deployment activities.&nbsp;</li><li>Contribute to platform standards, configuration best practices, and governance models.&nbsp;</li><li>Support audit and inspecting&nbsp;readiness by providing configuration evidence and explanations.&nbsp;</li></ul><p></p><p><strong>Qualifications and Skills:</strong>&nbsp;</p><p>We expect you&nbsp;to have&nbsp;+5 years of hands-on Veeva Vault configuration experience and experience working in a validated environment with change control. Furthermore, you have:&nbsp;</p><ul><li>A&nbsp;Vault Platform Certified Administrator&nbsp;or similar certification (requirement)&nbsp;</li><li>Deep understanding of Vault security models, workflows,&nbsp;lifecycles,&nbsp;and metadata.&nbsp;</li><li>Ability to translate business requirements into scalable Veeva configurations&nbsp;and&nbsp;integrations.&nbsp;</li><li>Experience supporting audits and inspections.&nbsp;</li></ul><p></p><p><strong>Key competencies:</strong>&nbsp;</p><p>We expect you to be&nbsp;a strong team&nbsp;player who wants to contribute to team collaboration. You have a can-do attitude and can thrive in an informal, open environment where we work agile.&nbsp;</p><p></p><p><strong>Travel:&nbsp;</strong>5-10&nbsp;days&nbsp;per year.&nbsp;</p><p><strong>Office:&nbsp;</strong>Tuborg Boulevard 12, 2900 Hellerup&nbsp;</p><p></p><p><strong>Apply now.</strong>&nbsp;</p><p>We evaluate applications when received, so we encourage you to apply as soon as possible. Please note that we conduct interviews on a rolling basis and reserve the right to remove the job posting at any time.   &nbsp;</p><p>To ensure your application is reviewed, please&nbsp;submit&nbsp;it through the specified platform - applications sent by email or other channels will not be evaluated. &nbsp;</p><p></p><p>For more details&nbsp;about the position or the company, please contact&nbsp;Lene Rhein Larsen,&nbsp;<a href="mailto:lrl@ascendispharma.com" target="_blank" rel="nofollow noreferrer noopener" class="external">lrl@ascendispharma.com</a>&nbsp;or Maribel Estrada,&nbsp;<a href="mailto:mae@ascendispharma.com" target="_blank" rel="nofollow noreferrer noopener" class="external">mae@ascendispharma.com</a>.&nbsp;&nbsp;</p><p></p><p>You can learn more about Ascendis by visiting&nbsp;our website&nbsp;<a href="http://www.ascendispharma.com/" target="_blank" rel="nofollow noreferrer noopener" class="external">www.ascendispharma.com</a>&nbsp;&nbsp;&nbsp;</p><p>Applications&nbsp;must be&nbsp;submitted&nbsp;in English and will be treated confidentially.&nbsp;</p><p>&nbsp;</p><p><strong>A note to recruiters:&nbsp;</strong>&nbsp;</p><p>We do not allow external search party solicitation.&nbsp;&nbsp;Presentation of candidates without written permission from the Ascendis Pharma HR team (specifically from: Talent Acquisition Partner or Human Resources Director) is not allowed.&nbsp;&nbsp;If this occurs, your ownership of these candidates will not be acknowledged.&nbsp;</p><p>&nbsp;</p>