Who we are
Abdera Therapeutics Inc. is a precision oncology company developing next-generation targeted radiation therapies- one of the most cutting-edge and highly promising areas of drug development. The company is built on a proprietary modular technology platform optimized for the delivery of radioisotopes to selectively destroy tumor cells while sparing healthy cells. Abdera is using this platform to enable the rapid development of a broad range of safe and efficacious therapies serving cancer patients with limited treatment options.
Abdera Therapeutics is growing rapidly and seeking key new team members who thrive at the cutting-edge of innovation. Come join us and be a part of the ground-breaking team set to unlock the power of targeted radiotherapy!
What we look for
At Abdera Therapeutics, we are looking for curious and committed individuals who are ready for the opportunity to transform the way people living with cancer can be treated. We are relentless in our focus to offer new hope to families facing devastating diagnoses. We are in search of team members who work collaboratively with a diverse group of colleagues, respectfully engaging one another while collectively and inclusively tackling any challenges we may face. We are building an exciting and fast paced company passionate about discovering and developing tomorrow\xe2\x80\x99s most innovative cancer therapies.
Abdera is seeking an Associate Director/Director, Antibody and Antibody-Conjugate Process Development, to lead process development of antibody and drug conjugation that advances the company\xe2\x80\x99s clinical programs. This role will be essential to ensure phase-appropriate process development and optimization of antibody and drug conjugate manufacturing of our novel oncology therapy candidates. The Associate Director/Director is responsible for process development and manufacturing of antibodies and antibody-chelate-conjugates and drive the related CMC elements throughout the product life cycle of antibody-based radiopharmaceuticals.
The role requires a strong technical background in biologics processing, primarily in the areas of cell culture, purification, and conjugation, as well as familiarity with critically relevant areas such as analytical characterization, formulation, and cell line development.
Strong CMC process development technical background and leadership skills is required. A successful applicant will have prior hands-on experience taking a novel cancer therapy through IND and into clinical trials, building process development team and lab, overseeing external CDMO work, and be comfortable in a fast moving and nimble culture.
Location of Work: San Francisco, CA or Vancouver, BC
Principal Responsibilities
Building Antibody and Antibody-Conjugate Process Development Capabilities
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