Junior Life Science Consultant

Qualitice; Madrid; A distancia; EUR 30.000 - 38.000; Jornada completa

Descripción de la vacante

An innovative consulting firm is looking for a Project Support Specialist to join their remote-first team. This role offers a unique opportunity to work in the pharmaceutical and IT compliance sectors, assisting with client projects and maintaining compliance processes. You'll gain hands-on experience in a structured environment while collaborating with senior consultants on high-impact international projects. With a competitive salary and a flexible schedule, this position is perfect for proactive individuals eager to launch their careers in consulting and compliance. Join a team that values work-life balance and professional growth!

Formación

• Fluent in German and English, with a proactive and organized approach.
• Interest in compliance and regulated industries like pharma.

Responsabilidades

• Assist with client projects and documentation.
• Support IT compliance and manage workflows.
• Coordinate client communication and team efforts.

Conocimientos

German Language Skills

English Language Skills

Organizational Skills

Detail-oriented Mindset

Interest in Regulated Industries

Herramientas

Microsoft Suite

Azure DevOps

Descripción del empleo

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 Project Support Specialist 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, 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

Our environment is remote-first with occasional on-site workshops (e.g., Barcelona, Germany, Switzerland). We offer a flexible schedule to support work-life balance. You will have the opportunity to learn from senior consultants on high-impact international projects and build your career in compliance, pharma, and IT. The position offers a 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: