We are seeking a highly motivated Scientist I to develop and optimize new methods and techniques that generate reliable, reproducible data in a timely manner. The ideal candidate will bring broad technical expertise and a strong understanding of core analytical disciplines to support the early-phase development of small molecule and peptide drug substance and drug product programs across preclinical and clinical stages.

This role will work closely within the global Analytical R&D organization and with cross-functional partners, including Process Chemistry, Process Engineering, Drug Product Development, Molecular Profiling and Drug Delivery, Quality Assurance, and CMC-Regulatory.

Responsibilities

• Responsibilities include method development, release and stability testing of small molecules and peptides while maintaining compliance with laboratory quality standards.
• Independently design and conduct critical experiments that further project goals.
• Document experimental activities and results in a compliant fashion using electronic data acquisition and management systems.
• Implement and may innovate new experimental protocols/techniques.
• Interpret results and draw conclusions from own multistage experiments, note significant deviations, then suggest, design, and pursue relevant experiments.
• Troubleshoot experiments and instrumentation.
• Understand relevant scientific literature and apply theoretical framework to solving problems within scientific discipline in a timely manner.
• Demonstrate skill in multiple techniques, as required, to suit the changing needs of research or development sciences.
• Understand the goal and maintain high proficiency in their projects as well as the overall program.
• Demonstrate technical proficiency in their field, preferentially in the analytical areas of quantitative and instrumental analysis.
• Perform routine and complex tasks competently and independently and generate reliable and consistent results.
• Raises the bar and is never satisfied with the status quo.
• Understand and comply with AbbVie safety, quality and regulatory policies and government regulations.