Lead Process/Project Engineer (Pharma/Biotech)

The candidate is responsible for Equipment Package Ownership (full lifecycle – Engineering Design, Build, Testing (FAT), Installation and Commissioning), including experience in commissioning and qualification of process equipment. Responsibilities: Good experience in upstream, downstream and Central services process operation and has experience in equipment design for process equipment. Oversee a team of Process Engineers (5 to 10 engineers) Responsible to ensure on-time delivery of packages including basic and detailed design, commissioning and qualification activities, including URS development, FAT, SAT, DQ, IQ, OQ and PQ. Ensure that the appropriate Quality standards are applied consistent with best practice and internal Quality Standards and expectations. Engage with project teams and motivate Process Engineers to deliver the project from conceptual through implementation phase, encompassing support for a wide range of engineering and construction requirements. Coordinates with different functions like manufacturing, project engineering team, validation and quality for implementation of changes associated with the project. Work independently and/or with the project manager to complete the engineering projects within schedule, budget and quality constraints. Any other task as assigned by Supervisor/Manager. About You: Advanced Degree in Chemical Engineering, Chemistry or equivalent. Process Engineer with at least 10-15 years of experience Able to manage a team of Process Engineers (5 to 10 engineers) In Biologics industry with understanding of cGMP requirements Should have Design experience at various stages of project (Base, Detailed design) Preferably handling the Autoclave, Glove box, CIP Skid during project phase Able to support Installation, Commissioning & Qualification activity at site. Any other task given related to Process. Location: Tuas