# (Senior) Director, Regulatory Affairs CMC at Braveheart

- Company: Braveheart
- What the company does: Advancing treatments to improve outcomes and quality of life for patients with hypertrophic cardiomyopathy and related heart conditions. Backed by a16z.
- Company website: https://www.braveheart.bio
- Type: Startups
- Level: Principal and up
- Location: San Francisco, CA or Remote or Hybrid
- Work setup: Remote
- Pay: $210K to $305K base salary per year (USD)
- Posted: 2026-10-20
- Apply by: 2026-12-04
- Apply: https://job-boards.greenhouse.io/braveheartbio/jobs/4459149009?utm_source=1752vc&utm_medium=careers
- Page: https://www.1752.vc/careers/jobs/braveheart-senior-director-regulatory-affairs-cmc/

## About the role

The (Senior) Director, Regulatory Affairs CMC will serve as the Global CMC Regulatory Lead and provide regulatory CMC leadership for Braveheart Bio’s HCM program. Reporting to the Vice President of Regulatory Affairs, this hands-on individual contributor will develop and execute the global CMC regulatory strategy that carries our lead asset from Phase 3 through registration, launch supply, and lifecycle management. Found on 1752vc Careers, the job board for startup and VC roles.

## What they're looking for

- Bachelor's degree required, advanced degree in a life science, pharmaceutical science, or related field (PhD, PharmD, or MS) preferred
- A minimum of 12 years in Regulatory Affairs CMC, including serving as the CMC Regulatory Lead for late-stage or commercial products
- Hands-on experience authoring and reviewing CMC sections for INDs/CTAs and marketing applications (NDAs/MAAs)
- Direct experience supporting commercial readiness, including process validation/PPQ, launch supply, and pre-approval inspection preparation
- Experience with technology transfer and site-to-site comparability
- Experience overseeing CDMOs from a CMC regulatory perspective

Tags: Regulatory

Source: 1752vc Careers, https://www.1752.vc/careers/jobs/braveheart-senior-director-regulatory-affairs-cmc/