Duration: 6 months to start

Job Description

• The client needs a Project Engineer to coordinate with key cross functional stakeholders to manage scope, schedule, and budget on multiple projects and/or initiatives including oversight of operational readiness activities to render capital investments ready for Clinical and Commercial GMP Cell and Gene Manufacturing.

• The Project Engineer will develop and maintain detailed project plans, organize project teams and assignments, coordinate activities to complete project goals, manage change controls, work with various internal teams (i.e. Functional Area Owners, Program PMO, Engineering PMO/AME, site facility and operations, QA, validation team, etc.) to align and manage activities and other related tasks.
• Previous experience project managing GMP biologics production projects, proficiency with regulatory requirements of aseptic manufacturing, cleanrooms and new or expansion manufacturing suite projects if required.
• Expert level proficiency with scheduling, process mapping as well as GMP Quality Systems tools is required.
• Ability to chair cross functional meetings, communicate status, progress and risks in a concise and audience appropriate manner.
• The Project Engineer should have proven ability to perform at a high level in a matrix reporting structure with a dynamic execution environment while remaining focused and even tempered.