- South San Francisco, California, United States
- On-site
- Full-time · Associate
- 3+ years
Support development, optimization, and scale-up of purification processes for drug substance GMP production in a lab-based, onsite environment.
Responsibilities
- Support development, optimization, and scale-up of purification processes through lab-based and scale-up lab operation activities
- Support transfer of purification processes to GMP manufacturing for clinical material production
- Execute routine purification development operations from harvest to UF/DF following established protocols
- Analyze and critique experimental results, document and promptly communicate significant deviations or unexpected results
- Prepare small to large batches of buffer solutions following batch record recipe
Requirements
- Bachelor’s degree in Chemical Engineering
- Bachelor’s degree in Biochemistry
- Bachelor’s degree in Chemistry
- Nice to have: antibody purification
- Nice to have: antibody-like molecule purification