Job Description & How to Apply Below
In this pivotal role, you will lead method development and validation at CDMOs for GMP biotherapeutics. As an Analytical Team Lead and Subject Matter Expert, you will work on processes from early human trials to commercial filings. Your contribution will enhance analytical control strategies for multispecific antibodies and ADC biotherapeutics across cross-functional teams.
Key Responsibilities:
• Manage method development for GMP biotherapeutics
• Serve as ATL and SME for analytical methods
• Support analytical control strategies for ADCs
• Troubleshoot technical issues and guide team members
• Author regulatory submission documents and updates
Requirements:
• Ph.D. in relevant field and 5+ years experience
• Proficiency in chromatography, ELISA, bioassays
• Expertise in potency assay and QC methods
• Strong knowledge of product development lifecycle
• Familiarity with IND and BLA filing processes
Transform biotherapeutic analysis with Zymeworks by leveraging your depth of knowledge and skills.
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Position Requirements
10+ Years
work experience
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