Associate Director, CMC Regulatory
Lyell Immunopharma · Seattle, Washington, United States
Posted 26 days ago · $190,000 to $230,000
or apply directly on Lyell Immunopharma's site. We never take the application ourselves.
Is this posting real?
- This role has been open
- 26 days Lyell Immunopharma's roles stay open a median of 26 days
- Reposted
- No
- Salary listed
- Yes 100% of Lyell Immunopharma's roles list one
- Ghost-job risk at Lyell Immunopharma
- high 5 stale, 0 reposted of 14 open
- Hiring momentum
- 20 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 Lyell Immunopharma's own greenhouse board since 2026-08-03. Full hiring picture for Lyell Immunopharma.
About this role
The Associate Director, CMC Regulatory will provide regulatory expertise throughout the lifecycle of cell therapy products, ensuring compliance with CMC regulatory requirements. Responsibilities include leading risk assessments, managing submission timelines, and collaborating with cross-functional teams to prepare regulatory documents. The role also involves maintaining knowledge of the regulatory environment and developing best practices for CMC regulatory processes.
- benefits
- 2/5
- freshness
- 4/5
- career value
- 4/5
- role clarity
- 4/5
- 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 Lyell Immunopharma as an employer.
What you need
- MSc or PhD within a scientific or related discipline
- A minimum of 8 years of experience in CMC regulatory affairs
- Proven track record in preparing, reviewing and executing CMC regulatory documents to support clinical studies and marketing applications
- Strong oral and written communication skills
- Ability to multi-task in a fast-paced start-up environment
- Detail-oriented while also retaining the ability to see the big picture.
Nice to have
- Experience with cell therapy
- Global regulatory experience
- Minimum 2 years management experience
- Familiarity with AI-assisted tools for regulatory writing and document drafting
What you get
- Salary range of $190,000 to $230,000 annually
- Opportunity to earn an annual bonus
- Eligibility to participate in Lyell’s Equity Incentive Plan
Worth weighing
- No specific details on the company's current projects or pipeline are provided
- The role may involve navigating a complex regulatory environment which can be challenging
- The salary range is stated as an estimate and may vary based on qualifications and experience
Summarised from Lyell Immunopharma's posting. Read the full original.
Listed by Lyell Immunopharma on their greenhouse job board, last confirmed open on 2026-09-17. PitchMeAI is not the employer.
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