Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? We are currently seeking an experienced Commissioning, Qualification & Validation (CQV) Project Manager in León, Spain. Lead and 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, test scripts, and summary reports ).
Collaborate with cross-functional teams ( Engineering, QA, Validation, Manufacturing ) to ensure compliance with GMP, regulatory guidelines, and project timelines .
Provide project updates and progress reports to stakeholders .
Bachelor's degree in Engineering, Life Sciences, or related field.
Ability to work independently and collaboratively in a project environment .
Fluent in English and Spanish ( written and spoken ).
PQE Group gives you the opportunity to work on international projects, improve your skills and interact with colleagues from all corners of the world.