Senior Project Manager, Global Regulatory Affairs - Sunnyvale

Company Description · It started with a simple idea: what if surgery could be less invasive and recovery less painful? Nearly 30 years later, that question still fuels everything we do at · Intuitive · . As a global leader in · robotic-assisted surgery · and · minimally invasive ...

Company Description · It started with a simple idea: what if surgery could be less invasive and recovery less painful? Nearly 30 years later, that question still fuels everything we do at Intuitive. As a global leader in robotic-assisted surgery and minimally invasive care, our t ...

· Company Description · It started with a simple idea: what if surgery could be less invasive and recovery less painful? Nearly 30 years later, that question still fuels everything we do at Intuitive. As a global leader in robotic-assisted surgery and minimally invasive care, ou ...

Bring more to life. · At Cepheid, one of Danaher's 15+ operating companies, our work saves lives—and we're all united by a shared commitment to innovate for tangible impact. · ...

Director, Global Regulatory Affairs (Oncology) · Location: South San Francisco, CA (Hybrid) · Remote: Can be considered · Compensation: $235-270K base + 20% bonus + equity · Target Start: Mid‑April · About the Company · Our client is a global, commercial‑stage biopharmaceutical c ...

We are excited to expand our multidisciplinary team of individuals focused on creating revolutionary medicines to address the unmet needs of patients. At Septerna we strive to embrace diversity of thought, expertise and background through collaboration. · ...

This innovative patient-focused commercial-stage biopharmaceutical company is seeking a Regulatory Affairs Director to lead the development and implementation of regulatory strategy for a key oncology asset. The company offers flexible work arrangements competitive compensation s ...

Revolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies to inhibit frontier targets in RAS-addicted cancers. The company's R&D pipeline comprises RAS(ON) Inhibitors designed to suppress diverse oncogenic variants of RAS p ...

Revolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies to inhibit frontier targets in RAS-addicted cancers. The company's R&D pipeline comprises RAS(ON) Inhibitors designed to suppress diverse oncogenic variants of RAS p ...

Revolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies to inhibit frontier targets in RAS-addicted cancers. As a new member of the Revolution Medicines team, you will join other outstanding Revolutionaries in a tireless ...

We are seeking a Director, Regulatory Affairs (Global Filing Lead). The Director of Regulatory Affairs is accountable for driving preparation & execution of global regulatory NDA/MAA filings for late-stage oncology programs at RevMed. They will manage end-to-end execution of the ...

Revolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies to inhibit frontier targets in RAS-addicted cancers. · The Senior Manager of Regulatory Affairs will provide project teams with regulatory advice and obtain and main ...

The Director of Regulatory Affairs (US Filing Lead) will drive preparation & execution of Regulatory NDA/MAA filings for late-stage oncology programs at RevMed. They will manage end-to-end execution of the dossier ensuring cross-functional coordination and effective communication ...

Revolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies to inhibit frontier targets in RAS-addicted cancers. The company's R&D pipeline comprises RAS(ON) Inhibitors designed to suppress diverse oncogenic variants of RAS p ...

Responsible for supporting regulatory compliance activities by preparing, assessing, and executing regulatory submissions to FDA, Notified Bodies, and other global regulatory agencies. · ...

We are seeking a Director of Regulatory Affairs for Companion Diagnostics (CDx) to define and lead the end-to-end global regulatory diagnostic strategy for our portfolio. · The Global Head of Regulatory Affairs for CDx will ensure synchronized drug–diagnostic co-development from ...

Revolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies to inhibit frontier targets in RAS-addicted cancers. The company's R&D pipeline comprises RAS(ON) Inhibitors designed to suppress diverse oncogenic variants of RAS p ...

The Regulatory Affairs Specialist is responsible for managing regulatory submissions and government interactions related to products requiring regulatory approval. · ...

We are seeking a Regulatory Affairs & Quality Specialist with experience in medical devices and international regulations. · ...

· The Regulatory Affairs Specialist is responsible for managing regulatory submissions and government interactions related to products requiring regulatory approval. · ...

We are seeking an experienced Regulatory Affairs Consultant to support sustaining activities for Class III medical devices. · Review, assess, and document regulatory impact of manufacturing, process, · Solid understanding of FDA regulations · ...