It & Compliance Consultant Life Sciences (Remote) - €40.000 - €50.000 A Year - Remote

Join Qualitice - Shape the Future of IT & Compliance Consulting in PharmaAre 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 doingContributing to digital transformation initiatives in pharma and life sciencesTaking ownership of IT compliance & Computer System Validation (CSV) activitiesCollaborating with cross-functional stakeholders in German- and English-speaking environmentsPreparing and reviewing validation lifecycle documentation (risk assessments, test plans, reports, traceability matrices)Supporting supplier qualification, system inventories, and structured risk assessmentsResearching, 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 processesWhat we’re looking for3-5 years of relevant experience in IT projects, or quality/ GxP /life sciences environmentsFluency in German and English (both required)Background in IT, informatics, engineering, or a related technical field - or strong technical affinityFirst experience in IT projects, quality environments, or structured documentation work is a plusFamiliarity with digital tools (e.G. Microsoft 365, Azure DevOps, SharePoint, Jira, or similar platforms)Interest in regulated industries such as pharma, biotech, or medical devicesBonus: Knowledge of GDP, smart manufacturing, data integrity (ALCOA+), or ISO standardsStrong analytical mindset, attention to detail, and structured working styleProactive attitude and willingness to take ownership and grow into more responsibilityWhy join Qualitice?Remote-first setup, with occasional in-person workshops in Germany, Switzerland, or SpainFlexible working hours within a performance-oriented but balanced cultureDirect exposure to senior consultants and global pharmaceutical clientsReal project responsibility early in your careerContinuous learning in high-demand areas such as CSV, data integrity, and GxP complianceCompetitive salary: €40K-€50K depending on experienceHow to applySend 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: **#J-*****-Ljbffr

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 doingContributing to digital transformation initiatives in pharma and life sciencesTaking ownership of IT compliance & Computer System Validation (CSV) activitiesCollaborating with cross-functional stakeholders in German- and English-speaking environmentsPreparing and reviewing validation lifecycle documentation (risk assessments, test plans, reports, traceability matrices)Supporting supplier qualification, system inventories, and structured risk assessmentsResearching, 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 processesWhat we’re looking for3-5 years of relevant experience in IT projects, or quality/ GxP /life sciences environmentsFluency in German and English (both required)Background in IT, informatics, engineering, or a related technical field - or strong technical affinityFirst experience in IT projects, quality environments, or structured documentation work is a plusFamiliarity with digital tools (e.G. Microsoft 365, Azure DevOps, SharePoint, Jira, or similar platforms)Interest in regulated industries such as pharma, biotech, or medical devicesBonus: Knowledge of GDP, smart manufacturing, data integrity (ALCOA+), or ISO standardsStrong analytical mindset, attention to detail, and structured working styleProactive attitude and willingness to take ownership and grow into more responsibilityWhy join Qualitice? Remote-first setup, with occasional in-person workshops in Germany, Switzerland, or SpainFlexible working hours within a performance-oriented but balanced cultureDirect exposure to senior consultants and global pharmaceutical clientsReal project responsibility early in your careerContinuous learning in high-demand areas such as CSV, data integrity, and GxP complianceCompetitive salary: €40K-€50K depending on experienceHow to applySend 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.