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Principal Research Scientist II, Biologics Drug Product Development

AbbVie

North Chicago, IL, United States permanent

Posted: March 20, 2026

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Quick Summary

The Principal Research Scientist II, Biologics Drug Product Development role involves leading the development of new biologics products in the immunology, oncology, and neuroscience therapeutic area, with a focus on delivering innovative medicines that address medical challenges for patients today and tomorrow. The job requires expertise in immunology, oncology, and neuroscience, as well as experience in drug product development and regulatory affairs. The successful candidate will be based in North Chicago, IL, and must be willing to work remotely.

Job 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.

Biologics Drug Product Development (Bio DPD), a part of Development Sciences within AbbVie’s R&D, is a global organization that is responsible for drug product formulation and process development, and definition of the product presentation for biologics (proteins, conjugates, peptides, neurotoxins etc.) and genetic medicine (AAV, LNPs, Cell Therapy).

AbbVie is seeking a highly motivated candidate for the position of Principal Research Scientist II, located in North Chicago, IL. We are seeking an accomplished scientist with a proven track record in biologics formulation development, characterization and automation. This position will be an integral part of the product development and CMC teams and will have strong collaborations with several stakeholders, including discovery research, analytical research and development, bioprocess development, devices and combination products development, product development science and technology, pilot plants and third-party manufacturers.

Key Responsibilities:

• Lead a group responsible for formulation screening and optimization for a wide range of complex biologics modalities, drug product presentations and routes of administration.
• Develop phase-appropriate formulation screening workflows using medium and high-throughput systems.
• Employ orthogonal analytical tools to characterize the biophysical properties and solution behavior of complex biologics modalities.
• Build, maintain and continuously improve data analysis and visualization workflows for high data volume formulation development experiments.
• Develop and implement AI/ML tools to model the impact of formulation parameters on product quality attributes to inform formulation lock decisions.
• Apply design of experiments (DoE) and advanced statistical analyses for formulation robustness and design space studies.
• Oversee the authoring of product development sections in regulatory filings and interactions.
• Support and/or lead digital transformation initiatives as it relates to biologics formulation development.
• Initiate and/or support scientific initiatives to drive innovation, continuously enhance capabilities and platforms, and improve business processes.
• Serve as a drug product team leader for one or more projects and represents Bio DPD in the cross-functional Product Presentation and Device Strategy Team (PPDST) and the CMC Team.
• Effectively and timely communicate development plans, risks, and mitigation plans to stakeholders and line management.
• Support due diligence for business development opportunities as formulation subject matter expert.
• Manage a team of 4-6 scientists and engineers (BSc to PhD level) including other drug product team leaders.
• Responsible for performance management, development plans, and recommendations for promotions and transfers for direct reports.

• Bachelors, Masters, or PhD in Pharmaceutics, Pharmaceutical Sciences, Chemistry, Bioengineering, Chemical Engineering, or related disciplines with 16+ (Bachelors), 14+ (Masters), or 8+ (PhD) years of relevant industry experience.
• Proven ability to solve critical scientific problems.
• Strong experience with biologics (proteins, conjugates, peptides and/or neurotoxins) pre-formulation, developability, formulation development and biophysical characterization.
• Hands-on experience in developing and deploying data science solutions for scientific problems.  
• Experience as CMC cross-functional matrix team leader.
• People management experience.

​​​​​​​Key Competencies:

• Deep scientific knowledge and significant hands-on experience with biologics formulation development and biophysical characterization.
• Experience and/or formal training/education in data science.
• Effectively communicates to influence without authority, drives technical excellence, and inspires continuous improvement.
• Builds strong relationships with peers and cross-functional partners to enable higher performance.
• Connects ideas from disparate fields, integrates data and information quickly, and takes risks to achieve the highest performance.
• Raises the bar and is never satisfied with the status quo.
• Creates a learning environment, open to suggestions and experimentation for improvement.
• Embraces the ideas of others, nurtures innovation and manages innovation to reality.

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

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