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?

AtQualitice, 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 motivatedJunior 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

• SupportingComputer 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 applyingregulatory 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 ******.

Tell Us About

Why you're interested in consulting

Your availability

Your language skills

Your preferred working location