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About the company:
- Braveheart Bio is a clinical-stage biopharmaceutical company focused on developing therapies for hypertrophic cardiomyopathy.
- The company has a strong financial foundation and a high-value late-stage asset, offering an opportunity for mission-driven professionals.
Role overview:
- The Senior Director leads quality compliance and risk management, reporting to the VP of Quality.
- This role manages vendor qualification, audit programs, inspection readiness, and data integrity across GxP activities.
Key qualifications:
- Requires a Bachelor's degree and 15+ years of pharma/biotech quality experience.
- Must have broad GxP expertise, strong judgment, and ability to manage complex risks in a fast-paced environment.
Braveheart Bio
Braveheart Bio is a clinical-stage biopharmaceutical company developing therapies for hypertrophic cardiomyopathy and other cardiovascular diseases. It has a proven leadership team, strong financial foundation, and a high-value late-stage asset, offering an opportunity for mission-driven professionals.