Descripción de la oferta
Join Qualitice – Junior IT & Compliance Consultant (Life Sciences)
Launch your consulting career in Digital Quality & Compliance.
Are you passionate about technology, digital transformation and the pharmaceutical industry? Do you want to work on international projects while learning from experienced consultants?
At Qualitice , we help leading pharmaceutical, biotechnology and medical device companies deliver compliant digital transformation programmes. Our projects combine IT, Quality, Compliance and Project Management in highly regulated environments.
We’re looking for a motivated Junior IT & Compliance Consultant (m/f/d) to join our growing team and develop into a future Computer System Validation (CSV), Computer System Assurance (CSA) or Digital Quality Consultant.
No prior CSV experience is required—we’ll provide comprehensive training and mentoring.
What you’ll be doing:
✅ Supporting Computer System Validation (CSV) and Computer System Assurance (CSA) projects
✅ Assisting with validation documentation, testing and quality reviews
✅ Supporting implementation projects for systems such as ERP, Veeva, LIMS, MES and eQMS
✅ Participating in GxP risk assessments, supplier assessments and Data Integrity activities
✅ Coordinating project tasks and collaborating with international client teams
✅ Researching and applying regulatory requirements such as GxP, GAMP® 5, Annex 11 and 21 CFR Part 11
✅ Supporting audit and inspection readiness activities
✅ Learning from experienced consultants while taking on increasing responsibility
What we’re looking for:
Bachelor’s or Master’s degree in one of the following:
- Computer Science
- Information Technology
- Engineering
- Life Sciences
- Pharmacy
- Biotechnology
- Biomedical Engineering
- Business Informatics
- or a related discipline
Strong interest in digital transformation, IT and regulated industries
Excellent analytical and problem-solving skills
Proactive, structured and eager to learn
Comfortable working in an international environment
Fluent English (required)
⭐ German is desirable and a significant advantage.
⭐ Knowledge of pharmaceutical processes, quality management or software validation is a plus, but not required.
What you’ll learn
- Computer System Validation (CSV) and Computer System Assurance (CSA)
- GAMP® 5 (Second Edition)
- GxP Compliance
- Data Integrity
- Risk Management
- Project Management
- Leading enterprise platforms such as SAP, Veeva, LIMS and MES
Why join Qualitice?
Work with leading international pharmaceutical, biotechnology and medical device companies
Flexible remote-first working model
✈️ Opportunities to travel across Germany, Switzerland and Europe
Structured mentoring by experienced senior consultants
Fast professional development with increasing responsibility
Join a growing specialist consultancy focused on Digital Quality & Compliance
Friendly, international and entrepreneurial team culture
Location
Remote (Europe) with occasional travel to client sites.
Candidates must be legally authorised to work within the European Union.
Compensation
Competitive salary based on experience, plus excellent opportunities for professional development.
How to apply
Please send your CV or LinkedIn profile together with a short introduction to jobs@qualitice.com .
Tell us about:
- Why you’re interested in consulting
- Your availability
- Your language skills
- Your preferred working location
