Associate Director, Chemical Development
Nurix · Brisbane, California, United States
Posted 14 days ago · $243,410.16 to $256,800
or apply directly on Nurix's site. We never take the application ourselves.
Is this posting real?
- This role has been open
- 14 days Nurix's roles stay open a median of 30 days
- Reposted
- No
- Salary listed
- Yes 83% of Nurix's roles list one
- Ghost-job risk at Nurix
- high 11 stale, 0 reposted of 30 open
- Hiring momentum
- 43 roles opened in the last 90 days ↑ up vs. the prior 90 days
- Last confirmed on the employer's board
- 2026-09-17
Measured from postings appearing on and disappearing from Nurix's own greenhouse board since 2026-08-03. Full hiring picture for Nurix.
About this role
The Associate Director, Chemical Development at Nurix Therapeutics is responsible for overseeing regulatory starting materials and drug substance manufacturing activities, including scale-up processes from preclinical development to commercialization. The role involves managing contract manufacturing organizations, ensuring compliance with regulatory standards, and leading process validation programs. Additionally, the position requires preparing regulatory submissions and technical documentation, with a significant amount of travel expected for project needs.
- benefits
- 1/5
- freshness
- 4/5
- career value
- 4/5
- role clarity
- 5/5
- pay transparency
- 5/5
Scored from the posting itself — how clearly the role is described, how much it says about pay and benefits, and how recently it was listed. Not a judgement of Nurix as an employer.
What you need
- Doctorate (PhD) in Chemical Engineering, Pharmaceutical Chemistry, Organic Chemistry, Pharmaceutics, Pharmaceutical Science, or related scientific discipline
- 5 years of industry experience in a pharmaceutical or biotechnology CMC/cGMP environment
- Development of safe, scalable, phase-appropriate routes of synthesis to drug substance targets
- Oversight of US and international contract manufacturing organizations for the manufacture of cGMP new chemical entity drug substances
- Authoring Module 3 Sections for IND/IMPD and/or NDA/MAA filings
- Knowledge of ICH Q7, FDA 21 CFR Part 210, 211 and EU GMP Volume 4 Part I and II guidelines
What you get
- Base salary of $243,410.16 to $256,800 per year
- Higher compensation may be available with advanced skills and/or experience
Worth weighing
- Up to 50% domestic and foreign travel is required, which may vary by project needs.
- The role involves significant regulatory responsibilities, which may add pressure and complexity to the position.
Summarised from Nurix's posting. Read the full original.
Listed by Nurix on their greenhouse job board, last confirmed open on 2026-09-17. PitchMeAI is not the employer.
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