The Scientist I will be working in operations of AbbVie’s Regulated Bioanalysis department. The primary responsibility will be supporting clinical and non-clinical projects by analyzing biological samples for drugs and metabolites under GLP regulation.  In addition, the individual will have opportunities to contribute to broader areas within QTAS as their experience and expertise warrants.

Key responsibilities include:

• Impact projects mostly through lab activities.
• Independently design and conduct critical experiments that further project goals.
• Interpret results and draw conclusions from own multistage experiments, note significant deviations, then suggest, design, and pursue relevant experiments.
• Maintain awareness of evolving trends in separations and mass spectrometry
• Use and manage biohazardous matrices (e.g., plasma, serum, urine, blood, etc.)
• Perform routine and complex tasks competently and independently and generate reliable and consistent results.
• Maintain and troubleshoot complex LC systems and ultra-sensitive mass spectrometers
• Understand relevant scientific literature and apply theoretical framework to solving problems within scientific discipline in a timely manner.