Azurity Pharmaceuticals is a privately held, specialty pharmaceutical company that focuses on innovative products that meet the needs of underserved patients. As an industry leader in providing unique, accessible, and high-quality medications, Azurity leverages its integrated capabilities and vast partner network to continually expand its broad commercial product portfolio and robust late-stage pipeline. The company’s patient-centric products span the cardiovascular, neurology, endocrinology, gastro-intestinal, institutional, and orphan markets, and have benefited millions of patients. For more information, visit www.azurity.com.
Azurity Pharmaceuticals is proud to be an inclusive workplace and an Equal Chance Employer. Azurity's success is attributable to our incredibly talented, dedicated team that focuses on benefiting the lives of patients by bringing the best science and commitment to quality into everything that we do. We seek highly motivated individuals with the dedication, integrity, and creative spirit needed to thrive in our organization.
Brief Team/department Description
The analytical team at R&D; is playing an important role in product development of various dosage forms. The analytical team involves different workflows like analytical method development, stability studies, involving method verifications at CMO/CTL and post filling activities.
This role is with Azurity R&D; Analytical Scientist, which required to work in product development team’s analytical method development, Formulation sample analysis, method verification, Compendial method evaluation, Stability sample analysis and instruments calibrations.
Principle Responsibilities
Follow Good documentation practices
Execution of analytical method development of Nitrosamine impurities using high end instrument and method validation parameters for developed method.
Execution of analytical method development for unknown impurity and Genotoxic impurity identification using HPLC-PDA/UV/ELSD