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Job Description & How to Apply Below
As part of a dynamic team, you will report to the Head of Process Development and engage in comprehensive processes from conceptualization to technical integration.
Your role will be key in conducting risk assessments and developing mathematical frameworks for optimal manufacturing practices in cell therapy.
Key Responsibilities:
• Lead design and implementation of cell processing workflows
• Conduct FMEA and PHA risk assessments for production
• Develop models using Design of Experiments methodologies
• Support technology transfer and clinical manufacturing
• Collaborate with Quality to define validation strategies
Requirements:
• M.S. or Ph.D. in Bioengineering or similar
• 6-8+ years of industry experience in biopharmaceuticals
• Expertise in complex fluidic systems and process characterization
• Comprehensive understanding of GMP regulations
• Excellent communication and problem-solving skills
Elevate bioprinting advancements at Aspect Biosystems by contributing your engineering expertise.
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Position Requirements
10+ Years
work experience
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