Senior Scientist I, Biologics Analytical R&D

AbbVie • North Chicago, IL

114d

About The Position

The Biologics Analytical R D (ARD) group at AbbVie plays a critical role in advancing our pipeline of next-generation biologic medicines. We develop and optimize analytical methods, provide data that drives product and process understanding, and enable the release and stability testing needed to bring innovative therapies to patients. We are seeking a highly motivated, hands-on scientist to support early-phase programs (Discovery through Phase I) with a focus on antibody-drug conjugates (ADCs) and potential emerging modalities (e.g., LNPs, siRNA). This role is ideally suited for someone who thrives in a fast-paced, collaborative environment and wants broad exposure across techniques, modalities, and development stages.

Requirements

• Degree in Analytical Development, Chemistry, Biochemistry, Biology, or related discipline: BS with 10+ years industry experience, MS with 8+ years industry experience, or PhD with limited to 0 years' industry experience (new graduates considered) with relevant laboratory experience.
• Strong background in protein/biologics analytical characterization, particularly HPLC and capillary electrophoresis methods.
• Experience in method development and validation; familiarity with GMP expectations for early-phase programs.
• Demonstrated ability to work independently, manage multiple projects, and drive deliverables to completion in a fast-paced environment.
• Strong interpersonal and communication skills with a track record of cross-functional collaboration.

Nice To Haves

• Supervisory or mentoring experience preferred but not required.

Responsibilities

• Independently design, develop, and qualify robust analytical methods (e.g., HPLC, iCIEF, CE) to support drug substance and drug product characterization, reference material qualification, and early-phase validation.
• Execute GMP and non-GMP testing for release and stability; deliver comprehensive data packages that inform formulation, process development, and regulatory strategy.
• Partner closely with Drug Substance (DS), Drug Product (DP), Regulatory Affairs, QA, and PDS&T to align analytical strategy with program needs.
• Anticipate challenges, critically evaluate new technologies, and champion innovative solutions that accelerate program progress.
• Author technical reports, regulatory documents, and publications; contribute to building reference standards, product control strategies, and IND/CTA submissions.
• Contribute to a collaborative lab environment, with opportunities to mentor junior scientists and expand expertise across multiple analytical platforms.

Benefits

• Paid time off (vacation, holidays, sick)
• Medical/dental/vision insurance
• 401(k) to eligible employees
• Short-term incentive programs
• Long-term incentive programs

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Industry: Chemical Manufacturing
• Education Level: Bachelor's degree