Associate Scientist, I - Analytical R&D

Job Description
AbbVie (NYSE:
ABBV) is a global, research-based biopharmaceutical company formed in 2013 following separation from Abbott. AbbVie combines the focus and passion of a leading-edge biotech with the expertise and capabilities of a long-established pharmaceutical leader to develop and market advanced therapies that address some of the world's most complex and serious diseases.
AbbVie Analytical Research &
Development (AnalyticalR&
D) is a global analytical sciences organization responsible for all CMC analytical activities related to the development of AbbVie's pharmaceutical products. Our scope includes AbbVie's diverse pipeline of innovative small molecule and therapeutic biologic medicines and spans from the selection of Discovery candidate molecules through the transition of analytical methods and testing to commercial labs to support product launch. We are building a world-class team of scientists and leaders who will drive the advancement of industry-leading analytical capabilities and make substantial contributions to advance AbbVie's pipeline of innovative medicines. Careers in AbbVie Analytical R&
D provide unique opportunities to work with global and cross-functional teams to drive exceptional science and innovative product development strategies. We are looking for diverse candidates with strong scientific and leadership experience to join the AbbVie Analytical R&
D team and can offer exciting and rewarding career opportunities for these candidates.
Role Overview
Within Small Molecule Chemistry and Manufacturing Control (CMC) Development, Analytical Research &
Development focuses on utilizing measurement scientists of analytical chemistry to inform the development of new chemical entities and the associated formulations dosed in a preclinical and clinical setting across a wide range of pipeline programs. The group is highly cross-functional and works closely with internal Analytical R&
D colleagues as well as colleagues within Discovery, Process Chemistry, Pharmaceutics and Drug Product Development.
Key Responsibilities
Responsible for performing method development and execution of methods (e.G. (U)HPLC with UV/Vis or MS detection, Karl Fischer titration, GC with FID or MS detection, dissolution, physical measurements, etc.) for the characterization and development of small molecule active pharmaceutical ingredients, intermediates, starting materials, pre-clinical formulations, and accelerated stability samples.
Independent and productive in performing lab work with team lead guidance, including, but not limited to, solution and sample preparations, stability studies, instrument maintenance, and buffer preparations, after appropriate training.
Troubleshoot basic technical issues with team lead guidance.
Responsible for efficiently processing and visualizing analytical data and summarizing basic trends within the data.
Responsible for maintaining and keeping an accurate laboratory notebook with high attention to detail.
Validate analytical methods and perform testing on clinical supplies, following current Good Manufacturing Practices (cGMPs).
Member of functional and cross-functional teams driving business initiatives, executing activities with team lead supervision and guidance.