Junior IT & Compliance Consultant

Qualitice; Barcelona; A distancia; EUR 30.000 - 45.000; Jornada completa

Descripción de la vacante

Qualitice seeks a Junior IT & Compliance Consultant to join its team, focusing on digital transformation in the pharma sector. This role requires a technical background or interest, fluency in German and English, and offers opportunities to work on impactful projects in regulated environments. Enjoy flexible hours and learn from experienced consultants.

Servicios

Flexible working hours

Work-life balance culture

Learning from senior consultants

Formación

• Proficiency in German and English required.
• IT or engineering background or strong IT affinity.
• Interest in pharma, biotech, and medical devices.

Responsabilidades

• Support digital transformation projects in pharma and life sciences.
• Assist with IT compliance & Computer System Validation (CSV).
• Collaborate with cross-functional teams.
• Participate in supplier qualification and risk assessments.

Conocimientos

Fluent in German

Fluent in English

Attention to detail

Proactive mindset

Educación

Background in IT, informatics, engineering or related technical field

Herramientas

Microsoft 365

Azure DevOps

SharePoint

Descripción del empleo

Get AI-powered advice on this job and more exclusive features.

Join Qualitice – Your Gateway to IT & Compliance Consulting in Pharma

Are you ready to kick-start your consulting career at the intersection of technology , compliance , and the pharmaceutical industry ? At Qualitice , we help global clients navigate digital transformation, ensure IT and GxP compliance, and drive high-impact projects in regulated environments like life sciences, biotech, and manufacturing.

We are looking for a Junior IT & Compliance Consultant (m / f / d) with a technical background or strong interest in IT , fluent German and English , and a desire to learn and grow in regulated industries . This is your opportunity to work on international projects that shape the future of digital healthcare, smart manufacturing , and quality systems .

What you’ll be doing

Supporting digital transformation projects in pharma and life sciences

Assisting with IT compliance & Computer System Validation (CSV) (training provided)

Collaborating with cross-functional teams in English and German

Supporting documentation, testing, and validation of IT systems

Participating in supplier qualification, system inventories, and risk assessments

Researching and applying regulatory frameworks (e.g. GxP, GDP, ISO)

Contributing to project coordination, QA activities, and internal workflows

What we’re looking for

Fluency in German and English (both required)

Background in IT, informatics, engineering , or related technical field — or strong IT affinity

Familiarity with digital tools (e.g. Microsoft 365, Azure DevOps, SharePoint)

Interest in regulated industries, especially pharma, biotech, and medical devices

Bonus : Knowledge of Good Distribution Practice (GDP) , smart manufacturing , or data integrity standards

Proactive mindset, attention to detail, and structured working style

Remote-first setup, with occasional team workshops in Germany, Switzerland, or Spain

Flexible working hours and a culture that values work-life balance

Learn from senior consultants and industry experts

Work on real-world projects that combine technology and regulatory compliance

How to apply

Send your CV and a short intro (no formal cover letter needed). Just tell us who you are and what excites you about this role!

Apply here : Seniority level

Seniority level

Entry level

Employment type

Employment type

Full-time

Job function

Job function

Information Technology

IT Services and IT Consulting

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