AR
Senior Manager, CMC Regulatory Affairs
San Diego, San Diego County
On-site
Full-time
$140K – $170K USD
2 days ago- Employment type
- Full-time · On-site
- Posted
- November 12, 2026
- Salary range
- $140,000–$170,000 USD per year
Hiring confidence: Some gaps · 67/100
Some signals are missing from this posting. It may well be genuine, but it is worth confirming the role is still open before you invest time in applying. How this is scored
Job Overview
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Arrowhead Pharmaceuticals, Inc. (Nasdaq ARWR) is a commercial stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the genes that cause them. Using a broad portfolio of RNA chemistries and efficient modes of delivery, Arrowhead therapies trigger the RNA interference mechanism to induce rapid, deep, and durable knockdown of target genes. RNA interference, or RNAi, is a mechanism present in living cells that inhibits the expression of a specific gen…
This role is based in San Diego, San Diego County. Arrowhead Pharmaceuticals is hiring for this full-time position through Jobily, where you can check how well your resume matches the posting before you apply.
What you'll do
- Lead CMC regulatory strategy and execution
- Develop and manage regulatory submissions for RNA therapeutic products
- Oversee chemistry, manufacturing, and controls documentation
- Ensure compliance with FDA and international regulatory requirements
- Collaborate with manufacturing, quality, and development teams
- Manage CMC regulatory affairs for biopharmaceutical products
- Guide regulatory submissions through FDA review
- Mentor and supervise regulatory affairs team members
What you'll need
- Extensive experience in CMC regulatory affairs
- Knowledge of RNA therapeutics or biopharmaceutical development
- Understanding of FDA regulations and submission requirements
- Experience with regulatory submissions (INDs, BLAs, NDAs)
- Strong technical and scientific background
- Experience managing regulatory teams or projects
About the Company
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