Join Qualitice – Shape the Future of IT & Compliance Consulting in Pharma
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.
What you'll be doing
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
Researching, interpreting, and applying regulatory frameworks (e.g. GxP, SOX, GMP, ISO standards, data integrity principles)
Contributing to project coordination, QA activities, and the continuous improvement of internal processes
What we're looking for
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
Strong analytical mindset, attention to detail, and structured working style
Proactive attitude and willingness to take ownership and grow into more responsibility
Why join Qualitice?
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
Competitive salary: €40K–€50K depending on experience
How to apply
Send your CV and a short introduction (no formal cover letter required). Tell us who you are and what motivates you to work at the intersection of technology and compliance.
Apply at: jobs@qualitice.com