Senior Scientist, Analytical Development and Quality Control - Early Phase

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

Job summary

The ideal candidate has advanced degrees and 8+ years (PhD) or 14+ years (BS/MS) in CMC, plus strong cross-functional and communications skills to drive late-stage programs.

Qualifications

• Advanced degree in Chemistry, Pharmaceutics, or related field.
• PhD with 8+ years or BS/MS with 14+ years CMC experience.
• Strong experience in drug product analytical development and validation.
• Experience with amorphous solid dispersions (ASDs) and/or lipid-based formulations.
• Experience in CDMO and contract testing lab oversight.
• Experience supporting regulatory submissions (e.g., IND, IMPD, NDA).
• Fluency with ICH guidelines, cGMPs, and pharmacopeial chapters.
• Ability to work effectively in a cross-functional environment.

Responsibilities

• Lead analytical method development validation and lifecycle management for drug product formulations.
• Oversee DP development, PPQ activities, and stability programs.
• Author and review analytical development reports for regulatory submissions.
• Support regulatory submissions and health authority responses.
• Collaborate with cross-functional teams to ensure alignment of analytical and QC strategies.

Skills

Analytical method development

CDMO oversight

Regulatory submissions

Cross-functional collaboration

Technical writing

Data integrity

cGMP knowledge

Education

Advanced degree in Chemistry, Pharmaceutics, or related field

PhD with 8+ years or BS/MS with 14+ years CMC experience

Job description

Senior Scientist, Analytical Development and Quality Control - Early Phase

Brisbane, CA

Company

Nurix Therapeutics is a clinical stage biopharmaceutical company focused on the discovery, development, and commercialization of targeted protein degradation medicines, the next frontier in innovative drug design aimed at improving treatment options for patients with cancer and inflammatory diseases. Powered by a fully AI-integrated discovery engine capable of tackling any protein class, and coupled with unparalleled ligase expertise, Nurix’s dedicated team has built a formidable advantage in translating the science of targeted protein degradation into clinical advancements. Nurix aims to establish degrader-based treatments at the forefront of patient care, writing medicine’s next chapter with a new script to outmatch disease.

Position

Nurix Therapeutics seeks an experienced Senior Scientist to join the Analytical Development and Quality Control group. The Senior Scientist will be responsible for drug product (DP) analytical development, including method development, oversight of method validation at CDMOs, and lifecycle management in support of Nurix’s oncology and inflammation & immunology (I&I) programs.

This position provides technical oversight of analytical method development, validation, and testing conducted at external CDMO/CRO partners. The Senior Scientist will author analytical development reports and IND/IMPD/NDA sections and support late-phase tech transfer and validation activities. This role will also contribute to analytical development for new drug products and dosage forms. The Senior Scientist will work closely in cross-functional teams to ensure alignment and integration of analytical and QC strategies across development stages.

The ideal candidate will have expertise in chromatographic and dissolution method development, stability studies, and phase-appropriate validation and control strategies, along with demonstrated experience supporting late-phase development and regulatory submissions.

This position is onsite at Nurix headquarters in Brisbane, CA.

Responsibilities:

• Lead analytical method development validation and lifecycle management for drug product formulations, including amorphous solid dispersions (ASDs) and lipid-based systems
• Support PPQ activities, commercialization, commercial QC, and lifecycle management for drug product analytical methods and control strategies
• Design and oversee DP development, registration batch, and commercial stability programs, including protocol development and trend analysis
• Author and review DP analytical development reports to support regulatory submissions, and marketing authorization
• Oversee and support analytical activities, including method development, validation, and QC testing conducted at CDMOs and contract testing laboratories (CTLs)
• Contribute to investigations (e.g., OOS, OOE, OOT), root cause analysis and CAPAs
• Perform critical review of analytical data, protocols, reports, specifications, and related documentation
• Trend stability data and support establishment of retest periods and shelf life using statistical methods
• Collaborate in the development and justification of material control strategies and specifications
• Author technical documents, including analytical development reports, specifications, validation and stability protocols/reports, certificates of analysis (COAs), and storage statements
• Author and review analytical sections of regulatory submissions (e.g., IND/IMPD/NDA)
• Collaboratively author responses to health authority requests for information
• Act as a key contributor to multidisciplinary teams, including Chemical Development, Pharmaceutical Development, Regulatory, Quality, Preclinical, Supply Chain, Medicinal Chemistry, and DMPK
• Maintain and organize analytical documentation and data to ensure traceability, data integrity, and inspection readiness
• Follow cGMP requirements and internal SOPs
• Travel up to 5%, as required

Qualifications:

• Advanced degree in a relevant discipline (Chemistry, Pharmaceutics, or related field)
• Senior Scientist: BS/MS degree with 14+ years or PhD with 8+ years of industrial CMC experience
• Strong experience in drug product analytical development and validation
• Experience with analytical development for amorphous solid dispersions (ASDs) and/or lipid-based formulations
• Experience in CDMO and contract testing lab oversight
• Experience supporting regulatory submissions (e.g., IND, IMPD, NDA) and global regulatory filings
• Fluency with ICH guidelines, cGMPs, and pharmacopeial chapters
• Ability to work effectively in a cross-functional environment
• Strong technical writing skills (e.g., development reports, regulatory documents)
• Ability to manage multiple priorities in a fast-paced environment
• Excellent communication and cross-functional collaboration skills

Salary Range: $162K – $186K