Sorrento Therapeutics Inc. is a fast growing, clinical stage, antibody-centric, biopharmaceutical company developing new therapies to turn malignant cancers into manageable and possibly curable diseases. Sorrento's multimodal multipronged approach to fighting cancer is made possible by its' extensive immuno-oncology platforms, including key assets such as fully human antibodies ("G-MAB library"), clinical stage immuno-cellular therapies ("CAR-T"), intracellular targeting antibodies ("iTAbs"), antibody-drug conjugates ("ADC"), and clinical stage oncolytic virus ("Sephrevir").
We attract smart people who play well with others. We're small enough for your ideas to make a big impact, and large enough to offer you opportunities to grow professionally at any stage of your career.
If you're a quick learner, enjoy working in the biotech industry, and share our mission of providing ground-breaking impact to medicine, each other, and our patients, Sorrento Therapeutics is the place for you!
WHAT YOU'LL DO:
The Scientist is responsible for the assay development, optimization and validation to support pre-clinical and clinical trials. This individual will also be responsible for ensuring that the process and/or product meets quality and regulatory requirements. This position plays an important role in the qualification/validation and successful transferring of assay methods from/to quality control personnel internally and at client sites.
ESSENTIAL DUTIES AND RESPONSIBILITIES:
Develops reliable biochemical and biological assays for process monitoring and/or product characterization
Communicates findings, presents data and conclusions openly and effectively
Reviews scientific literature and other technical publications to stay up-to-date and maintains expertise in assay development, cell biology and immunology
Writes development reports
Authors SOPs and Data Capture Forms
Develops and carries out assay qualification studies
Supports product and reference standard stability studies
Carries out in-process and drug product testing in support of biopharmaceutical product manufacturing and fill/finish activities
Provides scientific/technical guidance and decision-making as appropriate
EDUCATION AND QUALIFICATIONS:
PhD in biology, biochemistry, bio-engineering or related disciplines with 0-5 years experience; or Master's degree with greater than 8 years post-graduate or industrial experience
Experience with development of ELISAs, qPCR assays, and cell-based assays preferred
QC and operational experiences preferred
Strong problem-solving, troubleshooting, and organizational skills
Excellent oral and written communication skills
Ability to work independently and collaboratively with groups
Support scientists who are on the leading edge of immunotherapies for the treatment of cancer.
Earn a competitive salary that allows you to focus your attention on your passion.
A comprehensive benefits package including: medical, dental, vision, life and disability insurance, matching 401k, 10 paid holidays, and three-weeks' PTO, plus stock options.
If this sounds like the right career to fit your personality and interests, please apply, we're looking forward to meeting you!
Principals only. Recruiters, please don't contact this job poster.
Sorrento Therapeutics, Inc. is an Equal Opportunity Employer