Senior Director, Quality Compliance and Risk Management
Braveheart Bio · San Francisco, CA or Remote or Hybrid
Posted 19 days ago · $225k - $290k
or apply directly on Braveheart Bio's site. We never take the application ourselves.
Is this posting real?
- This role has been open
- 19 days Braveheart Bio's roles stay open a median of 20 days
- Reposted
- No
- Salary listed
- Yes 100% of Braveheart Bio's roles list one
- Ghost-job risk at Braveheart Bio
- high 3 stale, 0 reposted of 7 open
- Hiring momentum
- 11 roles opened in the last 90 days ↑ up vs. the prior 90 days
- Last confirmed on the employer's board
- 2026-09-17
Measured from postings appearing on and disappearing from Braveheart Bio's own greenhouse board since 2026-08-03. Full hiring picture for Braveheart Bio.
About this role
The Senior Director, Quality Compliance and Risk Management at Braveheart Bio will lead quality compliance initiatives, manage vendor oversight, and ensure inspection readiness. This role involves conducting GxP gap assessments, coordinating audits, and providing quality oversight for data integrity and computerized systems, while collaborating with various internal and external teams. The position requires extensive experience in quality risk management and compliance within the biopharmaceutical sector.
- benefits
- 1/5
- freshness
- 4/5
- career value
- 4/5
- role clarity
- 5/5
- pay transparency
- 5/5
Scored from the posting itself — how clearly the role is described, how much it says about pay and benefits, and how recently it was listed. Not a judgement of Braveheart Bio as an employer.
What you need
- Bachelor’s degree in life science, quality, engineering, or related discipline
- Minimum of 15 years of progressive pharmaceutical or biotechnology Quality experience
- Broad and substantive experience across multiple GxP disciplines
- Significant experience in Quality compliance, Quality Risk Management, inspection readiness, GxP auditing, and vendor oversight
- Demonstrated experience performing GxP gap analyses and compliance assessments
- Significant experience hosting and managing regulatory authority inspections
Nice to have
- Experience working in a small, rapidly growing, or startup pharmaceutical or biotechnology organization
- Experience supporting late-stage clinical development and regulatory submissions
- Experience evaluating in-licensed programs or data packages
- Experience with computerized system validation and IT Quality
- Experience with regulatory intelligence and evaluation of emerging GxP compliance expectations
What you get
- Base Salary Range: $225k - $290k
- Eligible for a competitive total rewards package, which may include an annual bonus, equity, and a comprehensive benefits offering
Worth weighing
- Role involves significant leadership and independent judgment in a complex regulatory environment
- Focus on GxP compliance and risk management may limit exposure to other areas of pharmaceutical development
- No specific mention of remote work flexibility beyond location options
- High level of experience required may limit opportunities for less experienced candidates
Summarised from Braveheart Bio's posting. Read the full original.
Listed by Braveheart Bio on their greenhouse job board, last confirmed open on 2026-09-17. PitchMeAI is not the employer.
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