Director, CMC Regulatory Affairs
Capricor Therapeutics, Inc.Highlight
Summary
About the Role
About You
- Bachelor’s degree in Pharmacy, Chemistry, Chemical Engineering, Life Sciences, or a closely related field.
- 8+ years of experience in regulatory affairs with a strong CMC focus in the pharmaceutical/biotech industry.
- Advanced degree (e.g., MS, PhD, PharmD).
- Experience with biologics, cell therapies, or regenerative medicine products.
Benefits
- Competitive salary range of $165k–$205k.
- Collaborative work environment that nurtures professional growth.
Capricor Therapeutics is a publicly traded (NASDAQ: CAPR) biotechnology company with a mission to develop groundbreaking therapies that make a meaningful impact on patients’ lives. Capricor is focused on the development of biologics, primarily cell and exosome-based technologies to treat or prevent a broad range of diseases. Our lead product is a cell therapy designed to treat Duchenne muscular dystrophy (DMD), the most severe form of muscular dystrophy, which results in muscle degeneration and premature death. Capricor’s innovative exosome technology is focusing on engineering exosomes to treat or prevent diseases with high unmet medical needs. Our translational approach to product development is based on the strong research foundation provided by our academic partnerships with leading scientists at top-tier research institutions.