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AbbVie

Sr Scientist I, QTAS

Posted 4 Days Ago
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In-Office
South San Francisco, CA, USA
97K-184K Annually
Senior level
In-Office
South San Francisco, CA, USA
97K-184K Annually
Senior level
Perform hands-on development, validation, and implementation of ligand-binding and multiplex biomarker assays (ELISA, MSD, SMCxPro, Olink). Establish pre-analytical workflows, run high-volume sample testing, analyze high-dimensional datasets, and communicate translational insights with cross-functional teams to support drug development programs.
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Company Description

About AbbVie

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.

Job Description

AbbVie is seeking a highly motivated and experienced scientist to join our Quantitative, Translation & ADME Sciences (QTAS) department in South San Francisco. The ideal candidate will have a strong background in immunology or immuno-oncology, along with expertise in biomarker assay development, particularly on ligand binding assay (LBA) platforms, to support multiple modalities in the drug development pipeline. The candidate will join the QTAS LBA team and should be a detail-oriented, self-driven scientist who thrives in a fast-paced, collaborative environment and is committed to delivering high-quality results across multiple projects under tight timelines. This role is primarily laboratory-based and includes hands-on experimental work as well as advanced data analysis. The successful candidate may also serve as the QTAS biomarker representative on project teams when ready, to collaborate with cross-functional partners both internally and externally for the successful execution of translational research strategies.

Core responsibilities include:

  • Performing laboratory experiments for the development, validation and implementation of biomarkers assays, using ligand binding assay platforms, including single and multiplex assays such as ELISA, MSD, SMCxPro, and Olink, etc.
  • Establishing and refining pre-analytical sample processing workflows, such as ex vivo stimulation and tissue homogenization, for the measurement of drug and/or biomarkers in unconventional sample matrices.
  • Performing high volume of sample testing and analyzing high-dimensional datasets using advanced analytical skills and apps.
  • Communicating and collaborating effectively with internal and external stakeholders with Discovery, QTAS, Pharmacology, and Precision Medicine teams to generate data and provide translational insights.

Qualifications

  • Master’s degree or equivalent education with typically 8 years of experience, or PhD with 0–3 years of experience. A background in immunology and cell biology is preferred, and experience in gene therapy is a plus.
  • Solid understanding of fit-for-purpose assay development and validation strategies in support of biomarker development with strong experience in LBA assay development; experience with flow cytometry is a plus.
  • Proficiency in data analysis and presentation using tools such as Prism and omics visualization software; experience with Python or R is preferred.
  • Highly motivated and results-oriented, with excellent communication and presentation skills, and the ability to work effectively both independently and as part of a team.
  • Passion for innovation, continuous learning, problem-solving, and applying new technologies to advance science.

Additional Information

​Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: ​

  • The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future. ​
  • We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.​
  • This job is eligible to participate in our short-term incentive programs. ​

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of  any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law. ​

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled. 

US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

https://www.abbvie.com/join-us/reasonable-accommodations.html

AbbVie Redwood, California, USA Office

Redwood, United States, United States

AbbVie San Francisco, California, USA Office

San Francisco, United States

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