Regulatory Operations Specialist
Maze TherapeuticsHighlight
Summary
About the Role
About You
- Bachelor's degree in a scientific or related discipline.
- 4+ years in regulatory operations or regulatory affairs with direct involvement in regulatory submissions.
- Experience performing QC review of published submission outputs and managing submission timelines.
- Familiarity with submission deliverables, version control practices, and submission lifecycle management.
- Strong organizational skills, attention to detail, and ability to manage multiple tasks concurrently.
- Strong written and verbal communication skills.
- Experience coordinating with external vendors or publishing partners.
Benefits
- Competitive medical, dental, and vision insurance.
- Mental health offerings.
- Equity incentive plan.
- 401(k) program with employer match.
- Generous holiday and PTO policy.
- Annual performance bonus eligibility.
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.