Biotechnology Research Jobs in South San Francisco, CA

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State And Local Government Affairs Manager

Zipline

profile South San Francisco - USA

Do you want to change the world Zipline is on a mission to transform the way goods move. Our aim is to solve the worlds most urgent and complex access challenges by building manufacturing and operating the first instant delivery and logistics system that serves all humans equally wherever they are....

10 days ago
Full Time

Senior Director Director, Cmc Regulatory Affairs

Oric Pharmaceuticals

profile South San Francisco - USA

Oversee and direct all CMC regulatory strategies in compliance with global regulatory requirements for the development of ORICs products.Provide CMC regulatory support for new and ongoing clinical trials e.g. manage/prepare CMC document packages in support of INDs CTAs and amendments to global regul...

30+ days ago
Full Time

Clinical Affairs Manager, In Vitro Diagnostics

Thermo Fisher Scientific

profile South San Francisco - USA

Work ScheduleStandard (Mon-Fri)Environmental ConditionsOfficeJob DescriptionLocation/Division Specific InformationThis position is part of the Regulatory and Clinical Affairs organization which ensures that the internal and external work performed to develop our in vitro diagnostics is in compliance...

30+ days ago
Full Time

Director, Regulatory Affairs (office Based 3xweek)

Zai Lab (us) Llc

profile South San Francisco - USA

The Director Regulatory Affairs is responsible for leading the development and execution of regulatory strategies for assigned assets ensuring alignment and execution across regions. This role collaborates closely with other regulatory team members to prepare and manage submissions leads interaction...

30+ days ago
Full Time

Director, Cmc Regulatory Affairs

Oric Pharmaceuticals

profile South San Francisco - USA

Oversee and direct all CMC regulatory strategies in compliance with global regulatory requirements for the development of ORICs products.Provide CMC regulatory support for new and ongoing clinical trials e.g. manage/prepare CMC document packages in support of INDs CTAs and amendments to global regul...

30+ days ago
Full Time