Principal Scientist - Microbial Bioprocess Development

F. Hoffmann-La Roche AG

South San Francisco (CA)

On-site

USD 121,000 - 224,000

Full time

12 days ago

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Benefits offered by this job

Relocation benefits

Job summary

Genentech is seeking a Principal Engineer/Scientist in Pharma Technical Development to lead scalable microbial (E. coli) process development for biologics. The role supports CCBO and collaborates across R&D, manufacturing, quality, and regulatory groups.

The position requires an advanced degree with extensive experience, strong communication, and the ability to drive cross-functional initiatives, including regulatory interactions and technology adoption. Relocation benefits apply.

Qualifications

  • Advanced degree in Chemical Engineering or related field with 8+ years (MS) or 4+ years (PhD) in E. coli or microbial process development.
  • Advanced technical experience in E. coli or other microbial process development, characterization and validation.
  • Strong written and verbal communication skills and ability to lead cross-functional teams.

Responsibilities

  • Develop scalable, robust, efficient, and sustainable microbial (E. coli) processes for biologics production.
  • Collaborate with research, manufacturing, quality, and regulatory functions on CMC deliverables.
  • Author regulatory filing sections and prepare responses for Health Authority Q&A.
  • Advocate for and influence stakeholders on new technology implementation.
  • Stay informed on industry trends and advancements in microbial process technology.

Skills

Cross-functional collaboration
Communication skills
Independent work ethic

Education

Master's degree in Chemical Engineering or related field
Ph.D. in Chemical Engineering or related field

Tools

Process simulation software
AI-based modeling tools
Regulatory documentation tools

Job description

Genentech is seeking a Principal Engineer/Scientist in Pharma Technical Development to lead scalable microbial (E. coli) process development for biologics. The role supports CCBO and collaborates across R&D, manufacturing, quality, and regulatory groups.

The position requires an advanced degree with extensive experience, strong communication, and the ability to drive cross-functional initiatives, including regulatory interactions and technology adoption. Relocation benefits apply.

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