Biotech CQV Consultant: Equipment Validation in Barcelona

A global leader in pharmaceuticals is seeking an experienced CQV Consultant in Barcelona. This position involves executing commissioning, qualification, and validation activities for equipment and systems in biotechnological production facilities. Candidates should have a Bachelor's degree in Engineering or Life Sciences, with at least one year of relevant experience in IQ/OQ/PQ protocols, as well as strong knowledge of GMP and FDA regulations. Fluency in Spanish and proficiency in English (minimum B2) are also required.
#J-18808-Ljbffr