Senior Director, Quality

Maze Therapeutics • South San Francisco, CA

3d • $257,000 - $314,000 • Hybrid

About The Position

Step into a pivotal role where science meets strategy. At Maze, we’re on a mission to uncover genetic insights and transform them into precision medicines that change lives. Our team is driven by curiosity, collaboration, and a commitment to improving treatment for people with severe diseases. We thrive on diverse perspectives and bold ideas, and we’re looking for someone who shares that spirit.
As our Head of Quality, you’ll shape and lead the Quality function at Maze, guiding strategy, systems, and compliance across our development programs. You’ll be instrumental in evolving our GxP processes and ensuring we’re inspection ready as we move into Phase 2 and beyond, with a focus on robust vendor oversight and building scalable systems to support late-stage and future commercial success.
Reporting to the Vice President of Regulatory and Quality Science, you’ll manage and develop two direct reports and foster a culture of collaboration, accountability, and continuous learning that extends across the organization.

Requirements

• Bachelor’s degree in a scientific discipline with 12+ years of progressive experience in biotech or pharma GxP quality assurance and compliance
• Deep knowledge of global GxP regulations, including U.S. CFR, EMA, ICH, and other relevant standards
• Proven experience in building and refining QA related systems that support clinical and commercial development
• Strong understanding of GMP Quality across raw materials, drug substance, drug product, labeling, packaging, and distribution, including testing, stability, and retention
• Experience enabling release of investigational and commercial materials in compliance with regulatory requirements
• Skilled in GxP training and implementation, with a focus on practical adoption
• Track record of leading and supporting regulatory inspections, including FDA, EMA, and global agencies
• Experience drafting audit responses and implementing CAPAs
• Proficiency in root cause analysis and CAPA management
• Familiarity with eQMS and eTMF systems
• Experience managing and developing direct reports, with a focus on mentorship and professional growth
• Collaborative mindset, with experience working across internal teams and external partners
• Strong strategic and organizational skills, with the ability to prioritize multiple projects
• Excellent leadership and communication skills (written and oral)
• High ethical standards with a positive, proactive, and solution-oriented approach
• Willingness to travel domestically and internationally for inspections, vendor oversight, and industry events

Responsibilities

• Be accountable for and evolve Maze’s GxP Quality strategy, providing leadership across internal operations and external partners, including CROs, CMOs, CTLs, and vendors supporting GxP activities
• Drive cross-functional integration of Quality across programs, ensuring timely engagement in key decisions
• Develop and implement risk-based Quality approaches for investigational materials, ensuring phase-appropriate systems from early development through commercialization, and proactively identify and mitigate quality risks
• Lead the development and continuous improvement of Quality Systems and SOPs supporting GxP activities
• Provide Quality oversight and input for regulatory submissions and correspondence, including INDs, IMPDs, CTAs, and interactions with FDA and global health authorities
• Provide Quality leadership for clinical programs, including oversight of CROs and clinical trial activities, ensuring GCP compliance and readiness for clinical inspections
• Partner strategically with CMC and lead GMP vendor oversight to ensure manufacturing, testing, packaging, labeling, and distribution activities comply with cGMP, FDA, ICH, EMA, and industry standards.
• Lead QA investigations, including product-impacting issues, and provide oversight and approval of CAPAs from deviations, complaints, recalls, audits, and inspections, ensuring timely and effective resolution and closure of findings.
• Drive Maze’s inspection readiness and serve as the lead Quality representative during health authority inspections
• Represent QA on cross-functional teams and company initiatives, providing Quality leadership and guidance in decision-making
• Stay current on evolving global regulations and industry best practices related to GxP and compliance, and apply these insights to strengthen Maze’s Quality frameworks and systems
• Develop and deliver GxP training across Maze, identifying opportunities for continuous improvement and embedding industry best practices into daily operations
• Oversee Document Control systems, ensuring compliance, consistency, and effective lifecycle management of Quality records

Benefits

• Maze offers a robust benefits package to our eligible employees including competitive medical, dental, and vision insurance, mental health offerings, equity incentive plan, 401(k) program with employer match and a generous holiday and PTO policy.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Number of Employees: 11-50 employees