Scientist I - Bio Process Purification Development at AbbVie · LumiJobs

Responsibilities

Develop, optimize, and scale up purification processes for monoclonal antibodies, multi-specifics, antibody-like molecules, and other complex biologic candidates across early- and late-stage drug substance process development; independently design and execute experiments, interpret results, and recommend next steps.
Support transfer of purification processes to GMP manufacturing sites for clinical material production, including preparation of technical documentation.
Evaluate novel, advanced bioprocess technologies that are in line with the group’s strategy
Plan and execute laboratory and scale-up activities efficiently, collaborating within the team and cross-functionally to meet project timelines and goals.
Work with contract laboratories to plan and execute assigned viral clearance studies, interpret results, and contribute to technical documentation.
Author technical reports and maintain complete, traceable experimental and batch records, including instrument and analytical data, in approved electronic systems; document results at execution and follow established procedures and timelines.
Prepare and deliver technical presentations and group-meeting updates; critically evaluate experimental results, communicate recommendations, and promptly document and communicate significant deviations or unexpected results
Follow applicable laboratory and scale-up facility safety procedures and standard operating procedures (SOPs), complete required training before performing assigned activities, and contribute to laboratory readiness through equipment maintenance, cleanliness, and inventory management
Bachelor’s degree with 5+ years of relevant industry experience or Master’s degree with typically 2+ years of relevant industry experience (in Chemical Engineering, Biochemistry, Chemistry, or a closely related field, preferred)
Must have protein purification experience including chromatography separations and filtration operations
Excellent attention to detail; ability to follow written experimental protocols and safety procedures and maintain accurate, complete, and traceable written records
Demonstrated ability to independently design, execute, and interpret critical experiments to answer scientific questions, troubleshoot purification operations, and recommend next steps

Scientist I - Bio Process Purification Development

Responsibilities

Qualification

Preferred

Benefits

Company

AbbVie

More roles at AbbVie