Full-time

Process and Clinical Validation Consultant

Posted by PQE Group • Spain, Catalonia, Spain

📍 Spain, Catalonia 🕒 February 28, 2026

About the Role

Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? PQE Group has been at the forefront of these industries since 1998 , with 40 subsidiaries and more than 2000 employees in Europe, Asia and the Americas.

We are currently seeking a Validation Consultant with strong expertise in Process Validation and Cleaning Validation to support pharmaceutical/biotech activities in Barcelona.

Responsibilities include, but are not limited to:

  • Plan, execute, and document Process Validation and Cleaning Validation activities
  • Author, review, and approve validation protocols and reports
  • Perform user reviews and ensure compliance with applicable GMP and regulatory requirements
  • Support and contribute to CSV (Computer System Validation) activities
  • Deliver training sessions on CSV and validation-related topics to internal teams and stakeholders
  • Collaborate with cro...

Ready to Apply?

Submit your application today and take the next step in your career journey with PQE Group.

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