Director or Senior Director, Regulatory CMC
Kymera Therapeutics · Watertown, MA
Posted 26 days ago · $195,000 – $330,000
or apply directly on Kymera Therapeutics's site. We never take the application ourselves.
Is this posting real?
- This role has been open
- 26 days Kymera Therapeutics's roles stay open a median of 43 days
- Reposted
- No
- Salary listed
- Yes 100% of Kymera Therapeutics's roles list one
- Ghost-job risk at Kymera Therapeutics
- high 17 stale, 0 reposted of 36 open
- Hiring momentum
- 44 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 Kymera Therapeutics's own greenhouse board since 2026-08-03. Full hiring picture for Kymera Therapeutics.
About this role
In this role, you will lead the development and execution of global regulatory CMC strategies for targeted protein degradation programs, focusing on late-stage development and approval processes. You will collaborate with various teams to ensure alignment of regulatory strategies with program timelines, author and review regulatory submission content, and provide strategic guidance to senior leadership. Additionally, you will oversee external manufacturing partners to ensure compliance and readiness for submissions.
- benefits
- 2/5
- 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 Kymera Therapeutics as an employer.
What you need
- BS, MS, or PhD in Chemistry, Pharmaceutics, Biochemistry, Chemical Engineering, or a related scientific discipline
- 10+ years of progressive Regulatory Affairs CMC experience in the biotechnology or pharmaceutical industry
- Deep experience in late-stage regulatory CMC activities
- Extensive hands-on small molecule CMC experience
- Demonstrated success independently authoring, reviewing, and managing CMC content for small molecule INDs/CTAs and marketing applications
- Strong working knowledge of global CMC regulatory requirements and guidance for small molecule products
What you get
- Competitive compensation package
- Eligibility for annual bonus
- Equity participation
- Comprehensive benefits
Worth weighing
- Role involves significant responsibility in regulatory strategy and compliance, which may be high-pressure
- Focus on late-stage activities may limit exposure to early-stage development processes
Summarised from Kymera Therapeutics's posting. Read the full original.
Listed by Kymera Therapeutics on their greenhouse job board, last confirmed open on 2026-09-17. PitchMeAI is not the employer.
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