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Director, GMP Quality Assurance

Maze Therapeutics · South San Francisco, CA · GMP Quality

Compensation

$219k – $267k /yr

Employment type

Full-time

Work setting

Hybrid

Location

South San Francisco, CA

Schedule

Day shift

Posted

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Job overview

The Director, GMP Quality Assurance role is hybrid in South San Francisco, CA, with an expectation of at least three onsite days per week. Compensation is $219,000–$267,000 per year, with eligibility for an annual performance bonus. Maze Therapeutics develops precision medicines using human genetic insights for patients with serious diseases. The director leads GMP Quality oversight across development programs and external manufacturing partners, supporting phase-appropriate execution and inspection readiness. The role also builds quality systems and develops the team as programs advance toward late-stage development and commercialization.

What you'll do

  • Provide GMP Quality oversight for development programs through commercial launch
  • represent GMP Quality on cross-functional teams
  • oversee external manufacturing and testing with Technical Operations
  • review batch records and support product disposition and release
  • lead investigations and resolution of deviations, complaints, audit and inspection findings, and CAPAs
  • develop and improve GMP quality systems, processes, and SOPs
  • support PPQ, technology transfer, and commercial readiness
  • manage and develop direct reports
  • support inspection readiness and regulatory inspections
  • travel domestically and internationally for inspections and vendor oversight.

What we're looking for

Skills & competencies
director
gmp quality assurance
biopharmaceuticals
small molecule drug development
quality systems
inspection readiness
capa
south san francisco ca
hybrid
$219k–$267k/year
annual bonus eligible
travel required
Work arrangement
  • Weekend coverage required

Benefits & perks

  • Medical, dental, and vision insurance, mental health offerings, equity incentive plan, 401(k) with employer match, holiday and paid time off policy.

Why this role

Hybrid schedule with at least three onsite days weekly; leads a small GMP Quality team and supports small-molecule programs advancing toward commercialization.

About the employer

Maze Therapeutics is hiring for this role. Industry: Research and Development in Biotechnology (except Nanobiotechnology). Sector: 54.

Additional details

Industry sector
54
Industry
Research and Development in Biotechnology (except Nanobiotechnology)
Occupation code
11-9199.00
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