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 an experienced Commissioning, Qualification & Validation (CQV) Consultant in Barcelona. This role will focus on the qualification and validation of equipment and systems in biotechnological production facilities .

Responsibilities include, but are not limited to:

• Execute commissioning, qualification, and validation activities for pharmaceutical/biotech equipment and systems .
• Prepare, review, and execute C&Q and validation documentation ( URS, DQ, IQ, OQ, PQ protocols , ...