IT Digital Advisor

Join Qualitice – Shape the Future of IT & Compliance Consulting in Pharma &##128640;

Are you ready to build your consulting career at the intersection of

technology, compliance, and the pharmaceutical industry ?

At

Qualitice

, we support global clients in navigating digital transformation, ensuring IT and GxP compliance, and delivering high-impact projects in highly regulated environments such as life sciences, biotech, and advanced manufacturing.

We are looking for an

IT & Compliance Consultant Life Sciences (m/f/d) with a technical background or strong IT affinity, fluent in German and English, and motivated to take ownership in regulated industries. This role offers exposure to international projects that influence digital healthcare, smart manufacturing, and quality systems — with real responsibility from early on.

Contributing to digital transformation initiatives in pharma and life sciences ✅ Taking ownership of IT compliance & Computer System Validation (CSV) activities ✅ Collaborating with cross-functional stakeholders in German- and English-speaking environments ✅ Preparing and reviewing validation lifecycle documentation (risk assessments, test plans, reports, traceability matrices) ✅ Supporting supplier qualification, system inventories, and structured risk assessments ✅ GxP, SOX, GMP, ISO standards, data integrity principles) ✅ Contributing to project coordination, QA activities, and the continuous improvement of internal processes

3–5 years of relevant experience in IT projects, or quality/ GxP /life sciences environments &##Fluency in German and English (both required) &##Background in IT, informatics, engineering, or a related technical field — or strong technical affinity &##First experience in IT projects, quality environments, or structured documentation work is a plus &##Familiarity with digital tools (e.g. Microsoft 365, Azure DevOps, SharePoint, Jira, or similar platforms) &##Interest in regulated industries such as pharma, biotech, or medical devices &##Bonus: Knowledge of GDP, smart manufacturing, data integrity (ALCOA+), or ISO standards &##Remote-first setup, with occasional in-person workshops in Germany, Switzerland, or Spain &##Flexible working hours within a performance-oriented but balanced culture &##Direct exposure to senior consultants and global pharmaceutical clients &##Real project responsibility early in your career &##Continuous learning in high-demand areas such as CSV, data integrity, and GxP compliance &##Tell us who you are and what motivates you to work at the intersection of technology and compliance.

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