Barcelona-Based Biotech CQV Specialist – GMP & Compliance

Talent is looking for an experienced Commissioning, Qualification & Validation (CQV) Consultant in Barcelona. The role focuses on qualifying and validating equipment and systems in biotechnological production facilities.

The ideal candidate will have a Bachelor’s degree in Engineering or Life Sciences and at least one year of experience in protocol development and execution in the pharmaceutical sector. Strong knowledge of GMP regulations is essential, alongside fluent Spanish and English skills.