Make a world of difference.
Join Nektar Therapeutics as we build the next generation of new and unique medicines to treat disease.

We are looking for energetic and talented people who like challenges, who want to make a difference and who have a track record of delivering results.

Recent Job Postings

Director, Regulatory Affairs

San Francisco, CA

Area of Interest: Regulatory Affairs
Job Type: Full Time

Responsible for oversight of regulatory activities of regulatory team. Develops strategies for earliest possible approvals of drug applications and device registrations. Ensures appropriate project/ program Regulatory support. Participates in higher level interactions with external partners. Formulates corporate responses to regulatory agencies and pharmaceutical group initiatives. Review of regulatory submissions and responses. Interacts with senior level regulatory personnel at partner companies and contract manufacturers.

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Sr. Scientist, Bioassay-Immunology/CMC

San Francisco, CA

Area of Interest: Bio-Analytical
Job Type: Full Time

Perform Bioassay method development, validation and oversee CMO activities to support CMC biological potency assays for product characterization, quality control and stability testing. Exercise technical discretion in the design, execution and interpretation of experiments that contribute to project strategies. Maintain a high level of professional expertise through extensive cell culture, bioassay development experience and regulatory knowledge of GMP biologics drug products. Work in a matrix system to support related functions such as CMC, PK, ADA and cell-based neutralization assays.

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Clinical Documentation Manager

San Francisco, CA

Area of Interest: Clinical Operations
Job Type: Full Time

Serves as the Development Operations resource to ensure required documentation exists to support regulated activities, including serving as the documentation technical specialist for other development functions contributing documents to the Trial Master File. Responsible for contributing to process design, implementation and hands on SOP, TMF and GCP document activities that ensure quality documentation and system performance. Proposes, implements and maintains appropriate control of the SOPs, TMF and manages necessary vendor oversight that includes performance and quality metrics.

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