Exelixis

Senior Principal Scientist (Antibody Drug Conjugate)

Exelixis$169K — $239K *
Pharmaceuticals & Biotech
11 - 15 years of experience
Job Overview by Ladders

Qualifications

  • BS/BA in Chemistry, Biochemistry, Chemical Biology or similar with 13 years of experience; or MS/MA with 11 years; or PhD with 8 years.
  • Hands-on experience in ADC conjugation chemistry from discovery to early CMC stages.
  • Demonstrated expertise in controlling drug-to-antibody ratio and optimizing product homogeneity.
  • Experience with site-specific conjugation platforms preferred.
  • Familiarity with dual-payload conjugates or bispecific ADCs is a plus.

Responsibilities

  • Design and execute ADC conjugation reactions to support discovery and early CMC deliverables.
  • Advance conjugation platforms and evaluate new methodologies for improved outcomes.
  • Optimize conditions to control drug-to-antibody ratios and minimize aggregation.
  • Characterize ADCs through advanced analytical techniques and interpret data for design decisions.
  • Lead scientific discussions on linker selection and contribute to candidate selection based on bio-functional assays.
  • Author technical reports and present findings to internal and external audiences.
  • Collaborate with cross-functional teams to meet project timelines and manage CRO relationships.

Benefits

  • 401k plan with company contributions.
  • Group medical, dental, and vision coverage.
  • Life and disability insurance.
  • Flexible spending accounts.
  • Discretionary annual bonus program and stock purchase opportunities.
  • 15 vacation days, 17 paid holidays, and 10 sick days per year.
Full Job Description
SUMMARY/JOB PURPOSE (Basic purpose of the job):

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 developability.
    • Help design and interpret in vitro bio-functional assays (efficacy, bystander, catabolite/metabolite ID, 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 reflects the cost of labor across several U.S. geographic markets, and we pay differently based on those defined markets. The base pay range for this position is $169,500 - $239,500 annually. The base pay range may take into account the candidate's geographic region, which will adjust the pay depending on the specific work location. The base pay offered will take into account the candidate's geographic region, job-related knowledge, skills, experience and internal equity, among other factors.

In addition to the base salary, as part of our Total Rewards program, Exelixis offers comprehensive employee benefits package, including a 401k plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts. Employees are also eligible for a discretionary annual bonus program, or if field sales staff, a sales-based incentive plan. Exelixis also offers employees the opportunity to purchase company stock, and receive long-term incentives, 15 accrued vacation days in their first year, 17 paid holidays including a company-wide winter shutdown in December, and up to 10 sick days throughout the calendar year.

WORKING CONDITIONS:

Our office is a modern space that fosters collaboration and creativity. Teams work closely together, sharing ideas and solutions in a supportive atmosphere. We provide all necessary equipment, including dual monitors and ergonomic chairs, to ensure a comfortable workspace.

DISCLAIMER:
The preceding job description has been designed to indicate the general nature and level of work performed by employees within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities and qualifications required of employees assigned to the job.

About Exelixis

Exelixis is a biotechnology company that develops and commercializes innovative medicines for the treatment of cancer. The company's flagship product, CABOMETYX® (cabozantinib), is an inhibitor of multiple tyrosine kinases, including MET, AXL, and VEGFR, which are involved in the growth and spread of cancer cells. CABOMETYX is approved in the United States for the treatment of advanced renal cell carcinoma (RCC) and hepatocellular carcinoma (HCC), and is also approved in the European Union and other countries for the treatment of advanced RCC. Exelixis is headquartered in Alameda, California, and has additional offices in South San Francisco, California, and Basel, Switzerland. Learn more at www.exelixis.com.
Learn more about Exelixis
Size
954 employees
Market Cap
$5 billion
Industry
Net Income
$111.7 million
5 Year Trend
+49.6%
Revenue
$987.5 million
NASDAQ

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