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 seeking a Process & Cleaning Validation Specialist with solid experience in pharmaceutical validation activities. The consultants will be involved in validation lifecycle management, supporting both routine and project-related activities in a GMP-regulated environment. Responsibilities include, but are not limited to: Execute and coordinate process validation and cleaning validation activities according to GMP requirements Draft, review, and approve validation documentation, including: Validation protocols, Risk assessments, Reports and SOPs and supporting documentation Support validation lifecycle activities from planning through execution and closure Collaborate with Production, QA, QC, and Engineering d...