Analytical Bench Scientist

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 Opportunity 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 Development department in the science organization at Azurity pharmaceuticals is responsible for developing the new analytical methods for the new dosage forms to ensure their quality.

Principle Responsibilities

This should specifically outline, in bullet form, the responsibilities of the job:

• Responsible for the development of analytical methods for product development, primarily for oral solutions, oral suspensions, and other oral dosage forms.
• Responsible for the preparation of method development reports, validation protocols and reports, and test methods.
• Accountable for performing routine analytical testing for assigned projects, as per requirements.
• Responsible for executing Analytical ATR (Analytical Testing Reports), documenting results, and sharing findings with the concerned formulation development (FD) team.
• Accountable for the calibration of assigned equipment, qualification of working standards, and maintenance of standards in accordance with storage conditions.
• Responsible for conducting forced degradation studies and identifying unknown impurities.
• Responsible for executing experiments to address and respond to regulatory queries.
  
  

Qualifications And Education Requirements

This section should include relevant qualifications and education requirements.

• 6-8 years of experience in Analytical Development of Formulation (primarily for oral solutions, oral suspensions, and other oral dosage forms)
• M. Pharm or MSc Chemistry
  
  

By applying for this role, you confirm that you are mentally and physically capable of fulfilling the job responsibilities detailed in the job description without any restrictions. If you have any concerns or even the slightest disability that may affect your ability to perform the job, please inform HR in advance.