KEY RESPONSIBILITIES
- Design and optimize LNP manufacturing processes by applying Quality by Design (QbD) principles and execute Design of Experiments (DoEs) to identify and control critical process parameters (CPPs)
- Optimize analytical methods such as DLS, Ribogreen, HPLC-CAD, IP-RP-HPLC, and endotoxin to identify and access critical quality attributes (CQAs)
- Interpret analytical data to assess process robustness and guide iterative development efforts
- Collaborate with internal teams to support process improvements and drive innovation
- Clearly present scientific findings and project updates in internal meetings and to external collaborators
- Drive technology transfer activities with external CDMO partners by preparing comprehensive technical documentation such as development reports, process summaries, and tech transfer packages to ensure successful external manufacturing
- Stay current with emerging trends in LNP technologies and contribute to strategic process improvements
- Track inventory, plan experiments, and contribute to an organized, quality-focused lab environment
REQUIRED QUALIFICATIONS
- Ph.D. in Chemical Engineering, Bioengineering, Pharmaceutical Sciences, Chemistry, or a related field with minimum of 3 years relevant industry experience; or M.S. with 6 years; or B.S. with 8 years
- Demonstrated expertise in LNP formulation and process development, including hands-on experience with microfluidic and high-shear mixing technologies, tangential flow filtration and dead-end filtration
- Proficiency in analytical characterization techniques for LNPs, including DLS, fluorescence-based assays and HPLC/UPLC methods (CAD, UV, IP-RP, SEC, IEX), including method development, troubleshooting, and data interpretation
- Experience with in-process and drug product stability studies
- Proven success in applying DoEs and statistical analysis tools for process optimization
- Experience supporting technology transfer of processes to external manufacturing environments, with a strong understanding of tech transfer best practices
- Demonstrated strong organizational skills
- A self-starter with demonstrated strong troubleshooting skills, capable of driving projects independently while contributing effectively in a collaborative, multidisciplinary environment
PREFERRED QUALIFICATIONS
- Knowledge of regulatory expectations for CMC development
- Familiarity with high-throughput screening methods
- Exposure to cell-based assays for LNP functional characterization
- Familiarity with data analysis tools and statistical methods such as JMP
- Experience with AAV vector process development or a strong interest and adaptability to learn viral delivery systems
BENEFITS
- Company-paid health/vision/dental benefits
- Unlimited vacation and generous sick time
- Company-sponsored meals and snacks
- Wellness, caregiver and ergonomics benefits
- 401(k) with company matching
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What We Do
Mammoth Biosciences is harnessing the diversity of nature to power the next-generation of CRISPR products. Through the discovery and development of novel CRISPR systems, the company is enabling the full potential of its platform to improve lives by reading and writing the code of life. Mammoth aims to democratize disease detection with an easy and affordable point-of-care test that allows real-time and simultaneous detection of multiple conditions. By leveraging its internal research and development and exclusive licensing to Cas12, Cas13, Cas14, and CasΦ, Mammoth can provide enhanced diagnostics and genome editing for life science research, healthcare, agriculture, biodefense and more. Based in San Francisco, Mammoth Biosciences is co-founded by CRISPR pioneer Jennifer Doudna and principal founders Trevor Martin, Janice Chen, and Lucas Harrington. The firm is backed by top institutional investors including Mayfield, NFX, and 8VC, Decheng and leading individual investors including Brook Byers, Tim Cook, and Jeff Huber.





