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Senior project manager it - digital quality systems (pharma/ life sciences)

Santa Margarida de Montbui
Qualitice
Publicada el 16 marzo
Descripción

Overview Senior Project Manager IT – Digital Quality Systems (Pharma / Life Sciences) – Remote (Europe). German & English required. Join Qualitice and lead high-impact digital transformation initiatives in the pharmaceutical industry. At Qualitice, we support global life sciences organizations in navigating digital transformation while ensuring regulatory compliance and operational excellence in highly regulated environments such as pharma, biotech, and advanced manufacturing. We are currently looking for a Senior Project Manager IT – Digital Quality Systems (m/f/d) to lead large-scale system implementations within the pharmaceutical sector. In this role, you will coordinate cross-functional teams and guide complex programs involving global stakeholders, regulated IT systems, and quality processes. This position is ideal for experienced professionals who enjoy working at the intersection of technology, compliance, and pharmaceutical quality systems.What you'll be doing Leading complex digital transformation projects in regulated life sciences environmentsManaging end-to-end implementation programs for enterprise quality systems and digital platformsCoordinating cross-functional teams across business, IT, quality, and validationManaging timelines, project risks, and stakeholder communication across international teamsDriving implementation governance including steering committees, status reporting, and escalation managementEnsuring alignment with regulatory requirements such as GxP, Annex 11, 21 CFR Part 11, and data integrity principlesOverseeing validation strategy and compliance activities related to regulated IT systemsSupporting change management, process harmonization, and global rollout activitiesWhat we're looking for 5+ years of experience in project management within pharma, biotech, or other regulated industriesProven experience managing IT system implementations (e.g., Veeva, SAP, Oracle, LIMS systems)Strong understanding of GxP environments, validation concepts, and quality processesExperience coordinating international project teams and multiple stakeholdersFluency in German and English (both required)Excellent communication, stakeholder management, and organizational skillsStructured and solution-oriented working style with strong risk awarenessNice to have Familiarity with Computer System Validation (CSV) and data integrity frameworks (ALCOA+)Experience working with global pharmaceutical organizationsWhy join Qualitice? Remote-first setup with occasional travel within EuropeWork on high-impact transformation programs for leading life sciences organizationsExposure to international projects and senior decision-makersA collaborative consulting environment where you can take real ownership of complex projectsContinuous learning in high-demand areas such as digital quality systems, CSV, and GxP complianceCompetitive salary: €50K–€70K depending on experienceHow to apply Send your CV and a short introduction (no formal cover letter required) to ******

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