Job Description

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, ...

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