Job Description

AbbVie Parenteral Product Development Science & Technology (PDS&T) is a global organization responsible for all CMC activities related to the development and commercialization of AbbVie's parenteral products.  Our scope includes AbbVie's diverse pipeline of innovative therapeutic biologics medicines, including monoclonal antibodies, antibody drug conjugates (ADC), and other novel modalities, and spans from clinical proof of concept through commercial product launch.  We are a world-class team of scientists and leaders driving the advancement of industry-leading analytical capabilities and AbbVie's pipeline of innovative medicines.  Careers in AbbVie Parenteral PDS&T provide opportunities to work with global and cross-functional teams to develop innovative products and drive exceptional science.

The Analytical Development group is responsible for programs that are transitioning from development stage to optimization and commercialization.  We lead final method development, optimization, and validation, ensuring all analytical methods are fit for use in commercial QC laboratories.  Key deliverables include product control strategies informed by analytical data and method understanding; robust analytical methods suitable for commercial QC labs; comprehensive data packages that drive product and process understanding; stability studies to establish commercial product dating; and approvable marketing application submission content.  This position will work primarily inside of the laboratory, providing testing support to meet Analytical Development’s deliverables for pipeline programs.

Responsibilities: 

Perform routine tasks competently with supervision and generate reliable and consistent results.

Demonstrate technical proficiency in multiple analytical techniques, including ability to resolve and troubleshoot routine scientific and technical issues, independently, as they arise.

Author technical documents (e.g., methods, protocols, reports, etc.), scientific publications, presentations.