Validation Technician

COMSER; Madrid; Presencial; EUR 30.000 - 40.000; Jornada completa

Descripción de la vacante

A leading pharmaceutical services provider in Madrid is looking for a Qualification & Validation Technician. In this role, you will manage validation projects, design and execute protocols, and analyze validation results. The ideal candidate has a scientific-technical background, at least 1 year of experience in validation, and strong analytical skills. This position offers a dynamic work environment with opportunities for growth.

Servicios

Personalized career development plan

Multidisciplinary team environment

Direct client interaction

Dynamic collaborative work environment

Formación

• Minimum 1 year of experience in equipment/process qualification and validation.
• Knowledge of aseptic environments is preferred.
• Professional level of English required.

Responsabilidades

• Manage validation projects from end-to-end.
• Design and execute validation protocols in compliance with GMP.
• Analyze and review validation results.

Conocimientos

Strong analytical skills

Organizational skills

Problem-solving skills

Knowledge of GMP regulations

Educación

Scientific-technical academic background (Chemistry, Pharmacy, Biology, Chemical Engineering or similar)

Descripción del empleo

At COMSER , we are expanding our GMP Compliance Services team and looking for a Qualification & Validation Technician to join us.

We are a company dedicated to supporting the pharmaceutical industry by accelerating the industrialization of new medicines that improve people's quality of life. Our focus is on injectable drugs manufactured in aseptic environments.

🔍 What we offer :

• A personalized career development plan in a growing company full of opportunities.
• A multidisciplinary team with scientific and engineering profiles, where creativity is valued.
• Direct interaction with clients throughout project execution.
• A dynamic and collaborative work environment.

🛠️ Key responsibilities :

• End-to-end management of validation projects.
• Design and execution of equipment and process validation protocols in compliance with GMP and client requirements.
• Analysis and review of validation results.
• Support to the business development team to drive growth in this area.

🎯 What we’re looking for :

• Scientific-technical academic background (Chemistry, Pharmacy, Biology, Chemical Engineering, or similar).
• Minimum 1 year of experience in equipment / process qualification and validation (preferably in aseptic environments).
• Strong analytical, organizational, and problem-solving skills.
• Knowledge of GMP regulations and lyophilization is a plus.
• Willingness to travel (national and international).
• Professional level of English.
• Own vehicle for client site visits.

At COMSER, we are committed to building an inclusive and diverse workplace where every individual can thrive and contribute their unique perspective.

📩 Interested in joining us? Send your CV — we’d love to hear from you!