OverviewIn this pivotal position, you’ll be the driving force behind global Quality applications, ensuring they remain compliant, user-friendly, and fit for purpose in a highly regulated environment.You’ll manage the full lifecycle of systems like Veeva QualityDocs, Veeva QMS, and LIMS—shaping solutions that meet business needs while enabling digital transformation. From gathering and translating requirements into actionable designs to coordinating system changes, testing, and validation, you’ll play a key role in harmonizing processes across the organization.Acting as the go-to expert, you’ll collaborate with stakeholders worldwide, resolve complex issues, and champion continuous improvement initiatives that make a real impact on healthcare innovation.QualificationsWe’re looking for a proactive professional with a strong “can-do” attitude and a passion for making things happen in a complex, regulated environment. You’ll bring:A Bachelor’s degree in IT, Business Informatics, Life Sciences, or equivalent.5–7 years of hands-on experience with Quality applications in the pharmaceutical or life-science industry.Practical experience with systems such as Veeva QualityDocs, Veeva QMS, LIMS or similar.Solid understanding of GxP requirements and validation principles.Proven experience in requirements management, change coordination, testing, and validation.Strong analytical and conceptual skills with the ability to translate business needs into pragmatic solutions.Fluency in English; additional languages are an asset.For further details, please contact Mark Bux-Ryan.
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