Senior Scientist I​/II - Biologics Analytical R&D

About Abb Vie

Abb Vie'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, neuroscience, and products and services in our Allergan Aesthetics portfolio.

Abb Vie Biologics Analytical Research & Development (Biologics Analytical R&D) is a global analytical sciences organization responsible for all CMC analytical activities related to the development of Abb Vie's pharmaceutical products. This team develops state‑of‑the‑art analytical techniques for therapeutic proteins and other biologic molecules. The role focuses on the development and implementation of analytical assays for complex biologics—including antibodies, antibody‑drug conjugates, and new modalities—using chromatography, electrophoresis, spectroscopy, and automated methods.

Successful candidates will contribute to assay development, testing, continuous improvement, and innovation within the group.

• Generate original technical ideas and research or development strategies as a scientist.
• Resolve key project hurdles and assumptions by utilizing available information and technical expertise.
• Lead method development and validation for complex biologic therapeutics.
• Research literature and incorporate findings into projects and the overall program.
• Collaborate with Discovery, Process Chemistry/Engineering, Formulation Development, and Characterization departments.

• Ph.D. in Biochemistry, Analytical Chemistry, Pharmaceutical Sciences or a closely related discipline, or an M.S. with 8 years of experience.
• Ph.D. with 0–4 years of experience (Senior Scientist I) or M.S. with 8 years of experience.
• Ph.D. with 4+ years of experience (Senior Scientist II) or M.S. with 10 years of experience.
• Strong knowledge in protein/oligonucleotide HPLC, capillary electrophoresis, MALS, automation, and/or spectroscopy for biologics.
• Previous cGMP or GLP experience and attention to detail in documentation.
• Demonstrated record of independent thought, creativity, and scientific accomplishment (e.g., peer‑reviewed journal publications, patents).
• Solid understanding of protein/oligonucleotide chemistry and biochemistry related to biologics drug development.
• Strong data and time organization/management skills and effective communication for collaborating with cross‑functional teams.
• Effective written communication of research and regulatory materials.
• Experience with multivariate analytical procedures development and/or validation is a plus.

• Compensation range is a range of possible base pay; actual compensation depends on multiple factors, including geographic location.
• This role offers a comprehensive benefit package, including paid time off, medical/dental/vision insurance, and a 401(k) plan.
• Eligibility to participate in short‑term incentive programs.

Abb Vie 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.