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.