This role supports development of equipment/pipe/pump sizing, mass flow and energy balances, and other engineering calculations, conducts site visits and field investigation for verification and data collection and other research for design, studies and reports, assists in preparing reports, technical documentation, and specification packages, and provides technical support during commissioning, qualification, and validation (CQV) efforts. The Process Engineer I is responsible for working under supervision to support the engineering, design, development, and implementation of process and clean utility systems for cGMP life science manufacturing facilities, pharmaceutical, biotechnology, animal health, and advanced therapy medicinal products (ATMP) industries.