Lead Drug Product Development Engineer

Nurix Therapeutics

Brisbane (CA)

On-site

USD 195,000 - 223,000

Full time

2 days ago
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Job summary

Nurix Therapeutics in Brisbane, CA seeks a Principal Engineer, Pharmaceutical Development Engineering to own hands-on engineering that turns a promising molecule into a manufacturable drug product. You will lead process development, scale-up, and CDMO operations for late-stage clinical and commercial programs.

This high-autonomy role requires expertise in GMP DP manufacturing, tech transfer to CDMOs, QBD and DOE studies, and regulatory CMC contributions.

Qualifications

  • Ph.D. in chemical engineering or related field with 8+ years in late-stage small-molecule DP development.
  • Extensive GMP DP manufacturing experience including spray drying, tableting, encapsulation.
  • Experience with tech transfer to CDMOs and QBD/DOE studies.
  • Strong cross-functional collaboration and regulatory familiarity (FDA/EMA/ICH).

Responsibilities

  • Provide engineering leadership for process development and scale-up for DP.
  • Oversee CDMO equipment engineering, tech transfer, and process validation.
  • Coordinate with QA, Development, and Supply Chain for timely DP release.
  • Contribute to regulatory filings (CMC sections) and inspection readiness.
  • Mentor scientists and engineers; travel up to 25%.

Skills

Process development
CDMO management
Tech transfer
DOE studies
QBD
GMP knowledge
Scale-up

Education

Ph.D. in chemical engineering or related field
M.S. in chemical engineering (or related field)
B.S. in chemical engineering (or related field)

Job description

Nurix Therapeutics in Brisbane, CA seeks a Principal Engineer, Pharmaceutical Development Engineering to own hands-on engineering that turns a promising molecule into a manufacturable drug product. You will lead process development, scale-up, and CDMO operations for late-stage clinical and commercial programs.

This high-autonomy role requires expertise in GMP DP manufacturing, tech transfer to CDMOs, QBD and DOE studies, and regulatory CMC contributions.

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