Validation Specialist (QA)

Rephine; Barcelona; Híbrido; EUR 40.000 - 60.000; Jornada completa

Descripción de la vacante

A leading quality assurance company in Barcelona is seeking a qualified individual to ensure GMP compliance and maintain Quality Systems documentation. The role requires a Bachelor’s degree in Chemical Engineering or a related field, alongside experience in a pharmaceutical GxP environment. Candidates must be fluent in Spanish and English, with strong teamwork and multitasking skills. This position offers a hybrid work model and opportunities for professional growth.

Servicios

Hybrid work model

Flexible hours

Shorter workday on Fridays

Formación

• Experience in a pharmaceutical GxP environment is essential.
• Project management experience is advantageous.
• Must possess a driver’s license.

Responsabilidades

• Validate facilities, equipment, and processes to ensure GMP compliance.
• Prepare and maintain Quality Systems documentation.
• Write procedures and work instructions for quality assurance projects.
• Assist in manufacturing process validation projects.

Conocimientos

Teamwork

Multitasking

Fluent in Spanish

Fluent in English

Educación

Bachelor’s degree in Chemical Engineering or related field

Descripción del empleo

Overview

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 worldwide.

Responsibilities

• Validate facilities, equipment, and processes to ensure GMP compliance.
• Prepare and maintain Quality Systems documentation.
• Write procedures and work instructions for quality assurance projects.
• Participate in qualification projects for facilities, process equipment, services, and control systems.
• Assist in manufacturing process validation projects.
• Contribute to projects across Spain and other international locations, including Europe and China.

Qualifications

• Bachelor’s degree in Chemical Engineering or a related field.
• Experience in a pharmaceutical GxP environment (Engineering, Maintenance, Validations, Production, or Quality Assurance).
• Strong teamwork and multitasking skills with the ability to handle multiple projects.
• Fluency in Spanish and English; other languages are a plus.
• Eager to learn, motivated, and passionate about Pharma Consulting.
• Project management experience is an added value.
• Must possess a driver’s license.

Benefits

Hybrid work model, flexible hours, and a shorter workday on Fridays to maintain a healthy work-life balance.

Global Exposure

Work with a multicultural team across multiple countries 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 company's future.

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.