As a Validation Engineer in the pharmaceutical industry, you will: Be responsible for the complete validation cycle (from design to validation) while ensuring compliance with GMP standards. Apply strong technical expertise in autoclaves and/or terminal sterilization processes. Identify improvement opportunities and support the integration of new technologies/methods to optimize processes. Draft essential documentation, including validation protocols, reports, FMEAs, and risk analyses. Collaborate closely with cross-functional teams (Production, Engineering, QA) to align outcomes and ensure clear communication. Manage records within the Quality Management System (CAPA, Change Control).
