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 cross-functional teams (QA, Production, Engineering, I...
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 cross-functional teams (QA, Production, Engineering, I...
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