Job Description

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...

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