Posted in: Other in Chicago | Posted: |
Job Description
Responsibilities:
● Apply analytical separation and detection modes for complex impurity profiling of pharmaceutical products to further the understanding of emerging cGMP manufacturing processes.
● Responsible for leading the analytical aspects of a project while working with other functional areas to advance projects through the development pipeline.
● Utilize understanding of a range of analytical techniques to conduct research and development studies related to small-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 and productive 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 research or 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 research or development activities and maintain a high level of productivity in the lab.
● Responsible for method development, testing procedures, and implementation of analytical control strategies to help the advancement of drug discovery candidates.
● 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.