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 looking for a Process & Cleaning Validation Specialist with solid experience in pharmaceutical validation activities. The selected consultant will be involved in validation lifecycle management, supporting both routine operations and project-related activities within a GMP-regulated environment. ‼️ Please note: for the first year, the role requires 100% on-site presence in El Masnou . Responsibilities include, but are not limited to: Execute and coordinate process validation and cleaning validation activities in compliance with GMP requirements Draft, review, and approve validation documentation, including validation protocols, risk assessments, reports, SOPs, and related supporting docum...