Principal Scientist I, Biologics Analytical Research and Development

AbbVie•San Francisco, CA

14h•Onsite

About The Position

AbbVie Biologics Analytical Research & Development (Biologics ARD) is a global analytical sciences organization responsible for CMC analytical development of AbbVie's pipeline of innovative therapeutic biologic products. We are a world-class team of scientists and leaders united by a shared mission to advance industry-leading analytical capabilities and meaningfully contribute to the advancement of AbbVie’s pipeline of innovative medicines. The Biologics ARD team at the AbbVie Bay Area site in South San Francisco has a long and rich history of biologics development. Located in a state-of-the-art facility housing end-to-end CMC development capabilities, the team works collaboratively to advance novel biologic therapeutics – including multi-specifics, ADCs, antibodies, and novel modalities – into first-in-human clinical development and through to clinical proof of concept. Careers in AbbVie Biologics ARD provide unique opportunities to work with cross-functional and global teams to drive exceptional science and innovative product development strategies. We are seeking a highly skilled and motivated analytical scientist to join the Biologics CMC Analytical Research and Development team. This role provides scientific leadership in the development of advanced analytical methods to support biotherapeutic protein characterization, process understanding, and product development. The successful candidate will independently develop innovative approaches and apply state-of-the-art capillary electrophoresis and chromatographic methods, serve as an analytical lead on development teams, and contribute to regulatory strategy and scientific innovation. This position also includes supervisory responsibilities, including leading and mentoring one or more scientists and supporting their performance and development. The role operates within a cross-functional, on-site environment supporting a portfolio that includes multi-specifics, antibodies, ADCs, and novel modalities.

Requirements

Degree in Chemistry, Biochemistry, Analytical Chemistry, or a related field.
PhD with 6+ years, MS with 12+ years, or BS with 14+ years of relevant industry experience.
Must possess a solid understanding of protein chemistry and biochemistry, particularly as it relates to biotherapeutic protein drug development.
Demonstrated expertise in analytical method development for biologics, with strong hands-on experience in capillary electrophoresis and HPLC.
Experience supporting biologics CMC development, QC method qualification/validation, and method transfer.
Proven ability to interpret complex data, solve technical problems, and propose innovative scientific solutions.
Experience contributing to regulatory submissions, including quality and characterization sections, and responding to health authority questions.
Strong leadership, communication, and collaboration skills, with experience mentoring and supervising scientists.
Must be capable of working in a fast-paced, collaborative environment and managing multiple concurrent projects with a high degree of independence.

Nice To Haves

Track record of scientific publications and conference presentations preferred.
Deep understanding of biologics analytics, impurity profiling, and protein characterization.
Ability to work effectively across functions and influence scientific and technical decisions.
Strong organizational skills and the ability to manage multiple priorities in a fast-paced environment.
Commitment to scientific excellence, quality, and continuous improvement.

Responsibilities

Independently develop state-of-the-art capillary electrophoresis and chromatographic methods to characterize biotherapeutic proteins and their associated variants and impurities.
Generate new scientific proposals and develop innovative approaches to solve difficult analytical challenges.
Represent the Biologics CMC Analytical Research and Development Group as Analytical Lead on CMC development teams and a subject matter expert on cross functional project teams.
Supervise a team of one or more scientists and be accountable for the effective performance of the team.
Develop/optimize, qualify/validate, and transfer fit-for-purpose QC release and stability methods.
Provide technical support and oversight for QC testing occurring at internal and external GMP laboratories.
Plan, author, and review regulatory submission documents, responses to health authority queries, technical reports, lab data, and method qualification/validation protocols.
Engage and influence the broader scientific community through publications and poster and oral presentations at industry conferences.