The Innovative Medicine Supply Chain (IM SC) is seeking a Project Engineer. The Project Engineer reports to the Engineering Design & Project Delivery Lead. This role is responsible for scoping and leading engineering projects within a pharmaceutical manufacturing environment (drug product), with a primary focus on aseptic compounding and filling. Example projects include the procurement of isolators, compounding and filling equipment, and/or supporting systems used in the production of parenteral drugs (e.g., parts washers, autoclaves, PUPSIT filter testers, CCIT testing equipment, etc.). Responsibilities Project Leadership Lead engineering projects, ensuring project scope, priorities, resources, capabilities, and processes are clearly defined and in place. Align with project sponsors and bring together core and extended teams to deliver the final project objectives. Prepare project intake documentation, including scope definition, business case analysis, alternatives assessment, and presentation of the recommended option for approval. Facilitate project planning, monitoring, and reporting against key deliverables and objectives. Apply standardized project management methodologies to ensure flawless project execution. Manage project finances: secure accurate budget allocation upon approval and control spending during implementation and post-project care. Oversee all technical engineering activities from conceptual design through construction and qualification, including coordination with internal resources and external contractors/suppliers. Identify and manage project risks using appropriate risk management techniques. Ensure sound technical engineering practices are applied throughout all phases of the project. Provide regular project updates to stakeholders including project sponsors, engineering leads, operations, and quality departments. Ensure full compliance with Environmental, Health, Safety, and Sustainability (EHSS) standards. Qualifications A technical education / degree in an engineering discipline is required. 2–5 years of experience in a relevant field is preferred. Experience in a GMP-regulated environment is a plus. Solid background in aseptic processing is highly desirable. Experience with risk-based qualification methodologies is an advantage.