A leading consulting firm in Murcia, Spain is seeking an experienced Commissioning, Qualification & Validation (CQV) Consultant. This role involves executing commissioning and validation activities for biotech equipment and systems, preparing necessary documentation, and ensuring compliance with GMP and regulatory guidelines. The ideal candidate holds a Bachelor’s degree in Engineering or Life Sciences and has at least 1 year of relevant experience. Proficiency in Spanish and fluent English (B2) is required.
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