Senior Director, Pharmaceutical Development

Maze Therapeutics•South San Francisco, CA

1d•$257,000 - $315,000•Hybrid

About The Position

As Senior Director of Pharmaceutical Development, you lead all small molecule drug product activities and serve as a technical expert overseeing processes at CDMOs. You guide formulation and process development, manage scaleups, and proactively identify risks, gaps, and solutions across CMC. You’ll dig into process and analytical data to resolve key challenges and advise on the best path forward. You bring strong cGMP expertise, support regulatory submissions, and collaborate across research, development, and technical operations. You coach teams for excellence, fuel intellectual curiosity, and champion inclusive, impactful leadership. This position reports to Vice President, Technical Operations. Maze Therapeutics is a clinical-stage biopharmaceutical company harnessing the power of human genetics to develop novel, small molecule precision medicines for patients living with renal, cardiovascular and related metabolic diseases, including obesity. The company is advancing a pipeline using its Compass platform, which allows it to identify and characterize genetic variants in disease and then link those variants to the biological pathways that drive disease in specific patient groups through a process it refers to as variant functionalization. The company’s pipeline is led by two wholly owned lead programs, MZE829 and MZE782, each of which represents a novel precision medicine-based approach for chronic kidney disease. Maze is based in South San Francisco. Maze is comprised of a team of passionate and creative professionals committed to discovering and delivering transformative medicines to patients suffering from both rare and common genetic diseases. We are fostering a culture that encourages vision, initiative and the development of talent. Our supportive work environment inspires creative thinking and freedom of expression, resulting in a stimulating atmosphere where people enjoy coming to work. While we have a passion for advanced science and pride ourselves on excellence in execution, ultimately, everything we do is about patients.

Requirements

PhD/MS/BS in Pharmacy, Pharmaceutics, Chemical Engineering, or related field.
15+ years of experience in Drug Product CMC development and manufacturing.
Deep expertise in small molecule Drug Product CMC from preclinical through commercial stages.
Experience leading Drug Product functions in biotech/pharma across multiple programs.
Strong knowledge of GMP and ICH guidelines; experience authoring regulatory submissions is a plus.
Proven success in tech transfer and scaleup.
Ability to strategically and pragmatically partner with CDMOs to optimize quality and operations.
Handson formulation development experience and the ability to share knowledge with external partners.
Strong attention to detail and a talent for building robust Drug Product processes.
Comfort navigating fast-paced, evolving startup environments.
A self-starter mindset with strong leadership, communication, and decision-making skills.
Willingness to travel as needed to support CMC goals with external partners.

Nice To Haves

Direct manufacturing experience preferred.

Responsibilities

Lead small molecule drug product formulation, process development, and manufacturing activities with external CDMOs.
Ensure drug products meet quality, cost, time, safety, and operational goals.
Evaluate CDMO capabilities and recommend approaches for development and manufacturing.
Drive formulation, process development, scaleup, and tech transfer from initiation through regulatory approval.
Shape and optimize CMC strategy, project plans, and execution.
Monitor daily CMC activities, resolve challenges, and ensure cGMP compliance.
Ensure CDMO processes meet needs across formulation development, tox studies, clinical trials, and commercial launch.
Assess and implement new methods, tools, and technologies that elevate program success.
Analyze scientific data, review batch documentation, and contribute to regulatory filings (IND/IMPD/CTA/NDA).
Review and approve master and executed batch records; lead process improvements and drive solutions.
Lead technical investigations, identify root causes, and implement corrective actions for deviations.
Collaborate effectively across teams with integrity, impact, and a values-driven mindset.
Represent Tech Ops and CMC in cross-functional settings.

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.

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