AGC Biologics
Overview
Project Engineer, Senior – AGC Biologics Location: Bothell, WA Schedule: Monday through Friday, 40 hours per week Compensation: $124,320 – $170,940 Responsibilities
Act as liaison between Operations, Technical Services, and Quality to coordinate project activities involving manpower, equipment, and facility space Lead project teams to develop plans, align resources, and deliver results meeting project scope, schedule, and budget Monitor key project metrics and track resource utilization and forecasts Ensure adherence to company, site, and FDA regulations, with a focus on cGMP compliance Manage project documentation, including plans, reports, and deliverables Participate in capital budget planning by proposing, justifying, and prioritizing projects Oversee and resolve technical issues or changes during project execution Provide regular project status updates to stakeholders and leadership Support facility and process design, technology transfer, and startup activities Mentor cross-functional engineering teams (mechanical, electrical, automation) Collaborate with Reliability Engineering to improve preventative maintenance programs Qualifications
Required
Bachelor’s degree in Chemical, Mechanical, Electrical, or Biotechnology Engineering 8+ years of relevant engineering and project management experience in biopharmaceutical or cell and gene therapy manufacturing Proven ability to manage capital projects up to $10 million Working knowledge of GMP documentation, facility and equipment validation, and process optimization Experience with process transfer and scale-up methodologies Proficiency with Microsoft Office and CMMS software Strong technical writing skills for reports and SOPs Preferred
PMP certification Lean Six Sigma certification Experience with upstream/downstream unit operations such as centrifugation, filtration, chromatography, bioreactors, CIP/SIP Experience with cell and gene therapy manufacturing facility design and construction About AGC Biologics
AGC Biologics is a leading global biopharmaceutical Contract Development and Manufacturing Organization (CDMO). Our network includes facilities in the U.S., Europe, and Asia. We are committed to delivering high-quality development and manufacturing of therapeutic proteins, plasmid DNA (pDNA), mRNA, viral vectors, and engineered cells. We are an equal opportunity employer committed to diversity and inclusion.
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Project Engineer, Senior – AGC Biologics Location: Bothell, WA Schedule: Monday through Friday, 40 hours per week Compensation: $124,320 – $170,940 Responsibilities
Act as liaison between Operations, Technical Services, and Quality to coordinate project activities involving manpower, equipment, and facility space Lead project teams to develop plans, align resources, and deliver results meeting project scope, schedule, and budget Monitor key project metrics and track resource utilization and forecasts Ensure adherence to company, site, and FDA regulations, with a focus on cGMP compliance Manage project documentation, including plans, reports, and deliverables Participate in capital budget planning by proposing, justifying, and prioritizing projects Oversee and resolve technical issues or changes during project execution Provide regular project status updates to stakeholders and leadership Support facility and process design, technology transfer, and startup activities Mentor cross-functional engineering teams (mechanical, electrical, automation) Collaborate with Reliability Engineering to improve preventative maintenance programs Qualifications
Required
Bachelor’s degree in Chemical, Mechanical, Electrical, or Biotechnology Engineering 8+ years of relevant engineering and project management experience in biopharmaceutical or cell and gene therapy manufacturing Proven ability to manage capital projects up to $10 million Working knowledge of GMP documentation, facility and equipment validation, and process optimization Experience with process transfer and scale-up methodologies Proficiency with Microsoft Office and CMMS software Strong technical writing skills for reports and SOPs Preferred
PMP certification Lean Six Sigma certification Experience with upstream/downstream unit operations such as centrifugation, filtration, chromatography, bioreactors, CIP/SIP Experience with cell and gene therapy manufacturing facility design and construction About AGC Biologics
AGC Biologics is a leading global biopharmaceutical Contract Development and Manufacturing Organization (CDMO). Our network includes facilities in the U.S., Europe, and Asia. We are committed to delivering high-quality development and manufacturing of therapeutic proteins, plasmid DNA (pDNA), mRNA, viral vectors, and engineered cells. We are an equal opportunity employer committed to diversity and inclusion.
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