Fluent in German and English is mandatory., Highly organized and detail-oriented with a proactive mindset., Interest in regulated industries such as GxP, GDP, and ISO standards., Familiarity with Microsoft tools and Azure DevOps is preferred..
Key responsibilities:
Assist with client projects, reports, and structured documentation.
Support IT compliance and Computer System Validation (CSV).
Help with client communication and team coordination, especially in German.
Manage workflows, deadlines, and internal processes, including risk assessments and supplier qualifications.
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Qualitice is a dynamic consulting agency for IT Quality & Compliance within the Healthcare industry founded by Anne Woitzik, MBA. The company caters for industries that need to follow strict regulations like biotech, chemicals, drugs, and medical devices.
Examples of Qualitice's consultant clients are major life science companies as well as small and medium-sized companies.
Qualitice develops and implements strategies for regulatory IT compliance and Quality topics within the Life Science Industry, such as Medical Device ,Pharmaceutical or Chemical companies.
Our services include:
Computer System Validation according to GAMP 5 and corresponding regulations
Project Management (SCRUM, SaFE, traditional)
Audit Execution and Preparation / Regulatory Compliance within Pharmaceuticals and Medical Device industry
Business and IT assessments
Strategy and advice on quality, validation and compliance
Requirement Engineering
Global and local SOP Creation, Review & Approval
Data Integrity Strategy & Gap Assessment (ALCOA)
Our Approach
Qualitice is flexible in the provision of its services, depending on your needs; either on-site, remotely, or a combination of both.
Join Qualitice – Your Gateway to Consulting & Pharma Are you looking to launch your career in consulting, compliance, and the pharmaceutical industry?
At Qualitice, we guide global clients through complex regulatory frameworks, support IT compliance initiatives, and manage high-impact projects across GxP-regulated environments.
We are currently seeking a Junior Consultant (m/f/d) with strong German and English language skills to support our projects, help maintain compliance processes, and ensure smooth operations.
If you're curious, proactive, and enjoy working in a structured environment, this is a great opportunity to gain hands-on experience in regulated industries like pharma and IT compliance.
What you'll be doing: Assisting with client projects, reports, and structured documentation Supporting IT compliance & Computer System Validation (CSV) (we'll train you!)
Helping with client communication (especially in German) and team coordination Managing workflows, deadlines, and internal processes Helping with system and equipment inventories, risk assessments, and supplier qualifications Researching regulatory frameworks and project-relevant standards Supporting workflows, testing documentation, and QA coordination and additional ad-hoc administrative tasks What we're looking for: Fluent German and English (both mandatory) Highly organized, detail-oriented, and proactive mindset Interest in regulated industries (e.G.
GxP, GDP, ISO standards) and IT compliance Comfortable with tools like the Microsoft suite, Azure DevOps Bonus: Experience with consulting, pharma, or quality management Why join Qualitice?
Remote-first with occasional on-site workshops (e.G.
Barcelona, Germany, Switzerland) Flexible schedule – we value work-life balance Learn from senior consultants on high-impact international projects Build your consulting career in compliance, pharma, and IT Competitive salary (€30K–€38K depending on experience) How to apply: Send us your CV and a short introduction (no formal cover letter needed) – just tell us who you are and why you're interested!
Apply here: ****
Required profile
Experience
Spoken language(s):
GermanEnglish
Check out the description to know which languages are mandatory.