Principal Research Scientist I

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.

The Principal Research Scientist I will be an integral part of the Late-Stage Process Analytics group within the Analytical Development team in the Operations – Product Development Science and Technology – Biologics division. The role involves supporting analytical aspects of biologics products with a focus on advancing AbbVie’s late-stage clinical programs. This position calls for an individual with a strong technical analytical background, demonstrated leadership skills and the ability to effectively communicate and work cross-functionally.

Serve as the process analytics lead for mab and DS in AbbVie's CMC teams, supporting late-stage biologics pipeline assets. Act as a partner to the process development groups. Balance stakeholder expectations to ensure effective collaboration. Serve as the subject matter expert for separation-based methods including HPLC and capillary electrophoresis for sample testing to support biologics mab and DS process development, characterization, validation as well as GMP manufacturing investigation activities. Evaluate and select effective analytical technologies and methods to meet program needs. Support timely delivery of high-quality testing results. Provide expertise and support for method development, execution, and troubleshooting. Provide hands-on support in the lab as needed. Review analytical results; communicate analytical issues and risks to relevant teams. Promote proactive risk resolution within and across functional areas to advance project objectives. Collaborate with other analytical teams in R&D and PDS&T on program transition, workflow and alignment. Participate in the preparation and review of technical documents for late-stage programs. Author and review analytical sections of IND/BLA filings. Demonstrate scientific excellence, advance science and innovation. Implement novel analytical techniques to enhance method robustness and expand analytical capabilities. Mentor and/or supervise junior scientists.

PhD in chemistry, biology, biochemistry, chemical engineering, or related technical discipline. Minimum of 6+ years (PhD) of relevant professional experience working in biotech/pharmaceutical setting. Proven experience with analytical activities supporting biologics development, including mAbs, multi-specifics, antibody-drug conjugates, and fusion proteins. Late-stage program experience preferred. Expertise in protein and impurity analysis techniques such as HPLC, capillary electrophoresis, and other relevant methods. Skilled in technical writing including experience in authoring, reviewing regulatory submissions and responding to agency information requests. Strong leadership skills and demonstrated ability to foster an engaging, inclusive and collaborative team environment. Excellent communication and interpersonal skills, effectively managing relationships to enhance team decision-making. Ability to work effectively across functions, anticipating and addressing overall program development needs. Ability to quickly comprehend and adapt to new situations, with an open mindset and can-do attitude, demonstrating agility where necessary to address evolving project needs. Ability to think critically and demonstrate troubleshooting and problem-solving skills. High attention to detail. Ability to lead and manage multiple projects of significant scope and