Senior Principal Scientist; Antibody Drug Conjugate
Job in
Alameda, Alameda County, California, 94501, USA
Listed on 2026-07-18
Listing for:
Exelixis, Inc.
Full Time
position Listed on 2026-07-18
Job specializations:
-
Research/Development
Biotech Research, Research Scientist, Drug Discovery, Regulatory Compliance Specialist
Job Description & How to Apply Below
## Senior Principal Scientist (Antibody Drug Conjugate)
Apply locations:
Alameda, CAtime type:
Full time posted on:
Posted Yesterday job requisition :
JR6987
** SUMMARY/JOB PURPOSE** **(Basic purpose of the job):
** Exelixis is expanding its Antibody-Drug Conjugate (ADC) platform to advance a growing pipeline of oncology bioconjugates. We are seeking a Senior Principal Scientist with deep expertise in conjugation chemistry to serve as the technical anchor for ADC generation, from discovery-scale screening through early process development and IND-enabling tox supply. You will operate independently at the bench, shape platform strategy, and partner cross-functionally with antibody engineering, linker-payload chemistry, analytical development, DMPK, and CMC.
** ESSENTIAL DUTIES/RESPONSIBILITIES:
*** Bioconjugation & Process Innovation + Design, execute and optimize ADC conjugation reactions at mg-to-multigram scale to support discovery screening, in vivo pharmacology and early CMC deliverables. + Apply and advance both stochastic (interchain cysteine) and site-specific conjugation platforms (engineered cysteine, transglutaminase, sortase, glycan remodeling, unnatural amino acids, native disulfide re-bridging); contribute to the evaluation and adoption of new platforms. + Optimize stoichiometry, linker chemistry, conjugation reaction conditions and buffer systems to control drug-to-antibody ratio (DAR), homogeneity, and aggregation.
+ Purify conjugates via FPLC, TFF/UF-DF, and preparative chromatography; develop and validate formulation buffers for bioconjugate stability.
* Analytical Characterization + Characterize ADCs by HIC, SEC, RP-HPLC, LC-MS (intact & reduced), and UV-Vis; interpret data to inform process and molecular design decisions. + Partner with analytical development to establish critical quality attributes (CQAs) and in-process controls for lead candidates.
* Scientific Leadership + Serve as the Biotherapeutics group’s conjugation subject-matter expert (SME) on program teams; provide the go/no-go technical read on lead molecule DAR strategy, linker selection, and develop ability. + Help design and interpret in vitro bio-functional assays (efficacy, bystander, catabolite/metabolite , MoA studies) in collaboration with biology and DMPK teams to enable candidate selection. + Author technical reports, patents and manuscripts;
present at program reviews and external scientific venues. + Track and integrate emerging conjugation technologies, linker-payload chemistries, and IP developments to shape platform investment.
* Collaboration & Delivery + Partner with Protein Science, ADC Chemistry, Analytical, DMPK, Toxicology and CMC/Process Development to deliver quality material on aggressive timelines. + Manage select CRO/CDMO relationships for outsourced conjugation, analytics or scale-up activities; support technology transfer. + Follow all IP, EH&S and laboratory compliance policies.
*
* SUPERVISORY RESPONSIBILITIES:
*** None.
** EDUCATION/EXPERIENCE/KNOWLEDGE &
SKILLS:
*
* Education:
* BS/BA degree in Chemistry, Biochemistry, Chemical Biology or related discipline and a minimum of 13 years of related experience; or,
* MS/MA degree in Chemistry, Biochemistry, Chemical Biology or related discipline and a minimum of 11 years of related experience; or,
* PhD in Chemistry, Biochemistry, Chemical Biology or related discipline and a minimum of 8 years of related experience; or,
* Equivalent combination of education and experience.
Experience:
Required
* Hands-on mastery of ADC conjugation chemistry from discovery through early CMC, with a track record of advancing molecules to development candidate nomination.
* Demonstrated experience in DAR control, product homogeneity optimization and formulation of bioconjugates.
Preferred
* Experience with site-specific conjugation platforms (e.g., engineered cysteine, THIOMAB, transglutaminase/AIICAP, glycan remodeling, sortase, click chemistry).
* Experience with dual-payload conjugates, bispecific ADCs or AOCs.
*
* Knowledge, Skills and Abilities:
** Required* Working knowledge of linkers (cleavable and non-cleavable), payload classes and their MoA.
* Fluency with HIC, SEC, RP-HPLC and LC-MS for conjugate characterization.
* Rigorous scientific problem-solving, excellent written and oral communication; proven collaborator across chemistry, biology and CMC.
* Excellent written and oral communication; proven collaborator across chemistry, biology and CMC.Preferred
* Familiarity with early process development, tech transfer, and CDMO management for GLP/GMP supply.
* Patents and peer-reviewed publications in bioconjugation.
* Working knowledge of ADC IP landscape.
** Work Environment
*** Modern, collaborative office and adjacent BSL-1/BSL-2 laboratory space at our Alameda, CA campus.
* Routine handling of proteins, organic solvents, and cytotoxic linker-payloads under standard EH&S controls.
* Travel up to 10% for conferences, CRO/CDMO site visits and collaborations.#LI-HG1### ### Our compensation…
Position Requirements
10+ Years
work experience
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