Associate Director, Regulatory Affairs - South San Francisco

· The Position:  · Maze Therapeutics is seeking a Manager, Regulatory Affairs to support the advancement of our clinical‑stage programs by contributing regulatory expertise and ensuring high‑quality execution of regulatory activities. In this role, you will collaborate closely w ...

The Position:  · Maze Therapeutics is seeking a Manager, Regulatory Affairs to support the advancement of our clinical‑stage programs by contributing regulatory expertise and ensuring high‑quality execution of regulatory activities. In this role, you will collaborate closely with ...

The Position · Maze Therapeutics is seeking a · Manager, Regulatory Affairs · to support the advancement of our clinical‑stage programs by contributing regulatory expertise and ensuring high‑quality execution of regulatory activities. In this role, you will collaborate closely wi ...

· Company Description · Zai Lab is a patient-focused, innovative, commercial-stage, global biopharmaceutical company based in China and the United States. We are dedicated to discovering, developing, and commercializing best-in-class and first-in-class therapies that address med ...

The Position · Maze Therapeutics is seeking a Manager, Regulatory Affairs to support the advancement of our clinical‑stage programs by contributing regulatory expertise and ensuring high‑quality execution of regulatory activities. In this role, you will collaborate closely with c ...

· Septerna is a biotechnology company based in South San Francisco, CA on a mission to develop life-changing medicines for patients with the vision to become the industry-leading G protein-coupled receptor (GPCR)-focused drug discovery company. The company's Native Complex Platf ...

The Director, Regulatory Affairs is responsible for leading the development and execution of regulatory strategies for assigned assets. · ...

Ohalo seeks an International Regulatory Affairs Lead to efficiently obtain regulatory approvals and registrations for new seed and plant varieties internationally. · Lead global regulatory operations for seed and plant variety launches. · Design efficient market-entry pathways. · ...

As an Associate Director, Regulatory Affairs you will provide regulatory expertise and executional leadership. · ...

· The Position:  · Join Maze Therapeutics as an Associate Director, Regulatory Affairs, where you will play a critical role in advancing our clinical-stage programs by providing regulatory expertise and executional leadership. As a key member of the development team, you will co ...

Ohalo is seeking an International Regulatory Affairs Lead to be responsible for efficiently obtaining regulatory approvals and registrations required to bring Ohalo's new seed and plant varieties to market internationally. · ...

Partnering with a high-growth clinical-stage biotech using human genetics to develop precision small-molecule medicines. · This is a hands-on Associate Director role supporting global regulatory strategy across multiple clinical programs. · ...

We're partnering with a high-growth, clinical-stage biotech using human genetics to develop precision small-molecule medicines across renal, cardiovascular and metabolic diseases. · This is a hands-on Associate Director role with real ownership — supporting global regulatory stra ...

· Job Summary: · We are seeking a highly motivated Regulatory Affairs Specialist to support the Regulatory Affairs department in ensuring compliance with the Presidio Quality Management System (QMS) and applicable regulatory bodies. In this role, you will be responsible for the ...

Job Summary: · We are seeking a highly motivated Regulatory Affairs Specialist to support the Regulatory Affairs department in ensuring compliance with the Presidio Quality Management System (QMS) and applicable regulatory bodies. In this role, you will be responsible for the tac ...

Marea Therapeutics is a clinical-stage biotechnology company seeking a strategic and hands-on Associate Director/Director, Regulatory Affairs to drive global regulatory strategy and execution for key development programs. · ...

The Regulatory Affairs Coordinator ensures the operational continuity of CAMICO by managing all corporate registrations, insurance licensing and regulatory filings. · High school diploma; 2+ years of administrative or coordinator experience. · ...

The Regulatory Affairs Specialist will support regulatory compliance activities by preparing and executing submissions to FDA and other global regulatory agencies. · ...

· PURPOSE OF JOB:  · This Regulatory Affairs Manager will work onsite in our San Mateo office 2-3 days a week. This position will support Route 92 Medical's efforts to sustain a best practice Quality System by ensuring compliance to regulatory requirements (13485:2016, MDSAP, EU ...

We are looking for a Regulatory Affairs Consultant to support several ongoing projects at about 10-20 hours per week. This role is remote. · Job Duties · Work closely with Pharmatech and our client's executive leadership team to lead the development of regulatory strategies and o ...