Environmental Validation Engineer

Rephine; Barcelona; Híbrido; EUR 35.000 - 50.000; Jornada completa

Descripción de la vacante

A leading Life Sciences company in Barcelona is seeking a Validation & GMP Technician. This position involves ensuring compliance with Good Manufacturing Practices (GMP) through validation and participating in quality assurance projects. The ideal candidate holds a Bachelor’s degree in Chemical Engineering and has experience in a pharmaceutical GxP environment. Fluency in Spanish and English is essential, with project management skills being a plus. The role offers hybrid working options and personal growth opportunities.

Servicios

Flexible hours

Shorter workday on Fridays

Global exposure

Dynamic work environment

Opportunities for growth

Formación

• Experience in pharmaceutical GxP environment.
• Project management experience is an added value.

Responsabilidades

• Ensure compliance with Good Manufacturing Practices (GMP).
• Participate in quality assurance projects.
• Assist in manufacturing process validation projects.

Conocimientos

Teamwork

Multitasking

Fluency in Spanish

Fluency in English

Educación

Bachelor's degree in Chemical Engineering

Descripción del empleo

Overview

Leading Life Sciences Quality Worldwide

At Rephine, we set the gold standard for quality assurance and GxP compliance in the Life Sciences industry. With offices in Barcelona, the UK, India, and China, we proudly support Pharmaceutical, Biotech, and Medical Device supply chains across the globe.

Are you passionate about Pharma and Life Sciences? Do you thrive in dynamic team environments and enjoy traveling for impactful projects? If you're ready to help a fast-growing global company enhance quality and compliance, we’re looking for a

Validation & GMP Technician

to join our team in Barcelona.

Responsibilities

In this role, you’ll be pivotal in ensuring compliance with Good Manufacturing Practices (GMP) through the validation of facilities, equipment, and processes as well as through the preparation of Quality Systems. Participating in quality assurance projects as writing procedures and work instructions.

Participating in qualification projects for facilities, process equipment, services and control systems.

Assisting in manufacturing process validation projects.

Contributing to projects across Spain and other international locations, including Europe and China.

Qualifications

You have a

Bachelor’s degree in Chemical Engineering

or a related field.

You’ve gained experience in a pharmaceutical GxP environment (Engineering, Maintenance, Validations, Production, or Quality Assurance).

You possess strong teamwork and multitasking skills, with the ability to handle multiple projects.

You are fluent in

Spanish and English

other languages are a plus).

You’re eager to learn, motivated, and passionate about Pharma Consulting.

Project management experience

is an added value.

Requirements

You must possess a driver's license. Take advantage of our hybrid work model, flexible hours, and a shorter workday on Fridays, allowing you to maintain a healthy balance between work and personal life.

Benefits & Growth

Global Exposure :

Work with a multicultural team across multiple countries, providing opportunities to expand your professional network and gain international experience.

Dynamic Work Environment :

Join a young, enthusiastic team where your contributions are valued, and your ideas can shape the future of the company.

Opportunities for Growth :

We provide a nurturing environment where your career can grow beyond expectations. For over 20 years, Rephine has been at the forefront of improving manufacturing quality processes for leading Life Sciences companies. Visit our career site to learn more and apply in English.