# Director or Senior Director, Regulatory CMC at Kymera Therapeutics

- Company: Kymera Therapeutics
- What the company does: Kymera is inventing a new generation of small molecule medicines by tackling the root cause of disease with targeted protein degradation. Backed by Bessemer.
- Company website: http://www.kymeratx.com
- Type: Startups
- Level: Principal and up
- Location: Watertown, MA
- Work setup: On-site
- Pay: $195K to $330K base salary per year (USD)
- Posted: 2026-08-21
- Apply by: 2026-10-12
- Apply: https://www.kymeratx.com/careers-culture/working-at-kymera/?gh_jid=7931045003#open-positions
- Page: https://www.1752.vc/careers/jobs/kymera-therapeutics-director-or-senior-director-regulatory-cmc/

## About the role

Kymera is a clinical-stage biotechnology company pioneering the field of targeted protein degradation (TPD) to develop medicines that address critical health problems and have the potential to dramatically improve patients’ lives. Kymera is deploying TPD to address disease targets and pathways inaccessible with conventional therapeutics.

## What they're looking for

- 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 (pivotal trials through NDA/MAA and post-approval) regulatory CMC activities
- Extensive hands-on small molecule CMC experience, including direct work on small molecule drug substance and drug product development, control strategy, and lifecycle management
- Strong working knowledge of global CMC regulatory requirements and guidance for small molecule products across the product lifecycle (FDA, EMA, ICH, and other regional health authorities)
- Experience with small molecule analytical method development/validation, specification setting, and post-approval change management

Tags: Development