Are you ready to join a world leader in the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? 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.
Execute and coordinate process validation and cleaning validation activities according to GMP requirements
Support validation lifecycle activities from planning through execution and closure
Collaborate with Production, QA, QC, and Engineering departments to ensure timely project execution
Support investigations related to deviations, non-conformities, and change controls
Ensure compliance with internal quality standards and international regulatory expectations
Participate in continuous improvement initiatives related to manufacturing and validation processes
Proven experience in Process Validation and Cleaning Validation within the pharmaceutical or biotechnology industry
Experience working in manufacturing environments under strict quality standards
Strong technical writing and documentation skills
Fluent in English and Spanish
xbhjioe PQE Group gives you the opportunity to work on international projects, improve your skills and interact with colleagues from all corners of the world.