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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