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Job Description & How to Apply Below
As a vital part of the Process Development, Biologics team, you will deliver technical recommendations for downstream protein manufacturing. This role requires a doctoral or master's degree, emphasizing hands-on experience in cGMP environments. You will guide cross-functional collaborations ensuring compliance with regulatory requirements, with a strong focus on critical quality attributes.
Key Responsibilities:
• Provide strategic recommendations for process development
• Create and oversee downstream development plans
• Guide technology transfer processes with stakeholders
• Author regulatory documentation and SOPs
• Support manufacturing operations and address NCR investigations
Requirements:
• Doctoral or Master's degree with 5-8 years experience
• Hands-on expertise in cGMP process development
• Proven track record in technology transfer
• Experience managing cross-functional projects
• Knowledge of antibody/protein production
Shape the future of biologic manufacturing at STEMCELL Technologies.
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Position Requirements
10+ Years
work experience
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