Senior Scientist, Drug Product Analytics & QC

Nurix; Brisbane (CA); On-site; USD 162,000 - 186,000; Full time

Job summary

Nurix Therapeutics seeks an experienced Senior Scientist to lead analytical method development and lifecycle management for drug product formulations, including work with ASDs and lipid-based systems. The role includes oversight of CDMO activities and contribution to regulatory submissions.

The position requires strong technical writing skills, experience with regulatory filings (IND/IMPD/NDA), and collaboration across Development, Regulatory, and QC teams. Onsite in Brisbane, CA.

Qualifications

• Strong experience in drug product analytical development and validation.
• Experience with amorphous solid dispersions (ASDs) and/or lipid-based formulations.
• Oversight of CDMO and contract testing labs.
• Experience supporting IND/IMPD/NDA and global filings.
• Fluency with ICH guidelines and pharmacopeial chapters.
• Excellent cross-functional collaboration and technical writing skills.

Responsibilities

• Lead analytic method development validation and lifecycle management for DP formulations.
• Oversee testing at external CDMOs and contract labs.
• Author analytical development reports and regulatory submission sections.

Skills

Analytical development

Validation

CDMO oversight

Regulatory submissions

ICH cGMP

Technical writing

Education

BS/MS in Chemistry/Pharmaceutics

PhD in related field (optional)

Job description

Nurix Therapeutics seeks an experienced Senior Scientist to lead analytical method development and lifecycle management for drug product formulations, including work with ASDs and lipid-based systems. The role includes oversight of CDMO activities and contribution to regulatory submissions.

The position requires strong technical writing skills, experience with regulatory filings (IND/IMPD/NDA), and collaboration across Development, Regulatory, and QC teams. Onsite in Brisbane, CA.