Responsible for method development, testing procedures, and implementation of analytical control strategies to help the advancement of pipeline candidates.

Leads the analytical aspects of a project including method development and validation, control strategy development, specification justification, data generation, regulatory submissions, technology transfer, and investigations.

Apply analytical separation and detection modes for complex impurity profiling of pharmaceutical products to further the understanding of emerging cGMP manufacturing processes.

Utilize understanding of a range of analytical techniques to conduct research and development studies related to synthetic molecule drug products, active pharmaceutical ingredients, intermediates, starting materials, impurities and impurity profiling.

Support new product development with advanced methods development and validations, technical transfer packages, and generation of technical data in support regulatory requirements.

Highly autonomous in performing laboratory research or method development, requiring only minimal direction from or interaction with supervisor.

Formulate conclusions and design follow-on experiments based on multidisciplinary data.

May initiate new areas of investigation that are scientifically meaningful, reliable, and can be incorporated directly into a development program.

Process, interpret, and visualize data to facilitate project team decisions.

Communicate and collaborate with cross-functional groups and departments.

Routinely demonstrate scientific initiative and creativity in development activities and maintain a high level of productivity in the lab.

Understand and adhere to corporate standards regarding code of conduct, safety, appropriate handling of materials, controlled drug and radioactive compounds, and GxP compliance, where applicable.

Senior Scientist I, Analytical Chemistry

Responsibilities

Benefits

Company

AbbVie

More roles at AbbVie