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.

We have an exciting opportunity—the person we select for this role will play a key part in Azurity’s digital transformation!

Principle Responsibilities

• Working experience in analytical research and development lab with hands on experience of Method development, Stability analysis of Solid Oral (tablets, Capsules), Injectable products, Oral suspension and Oral solution/Ophthalmic suspension/solution products.
• Carry out analytical method development and pre-validation involved in assigned projects, protocols & reports, in compliance with QMS to achieve the objectives as per project requirements.
• Carry out & Ensure Analytical support for formulation development, optimization & scale-up, as applicable to achieve the objectives as per project requirements.
• Support Analytical method validation and method transfer involved in assigned projects to achieve the objectives as per project requirements.
• Awareness on GLP, GDP, Data integrity and Documentation practices in lab work.
• Preparation of SOP, Test methods, Validation/Transfer protocols and reports knowledge is added advantage.
• Good knowledge and exposure on Related test and impurity profile methods development is needed.
• Knowledge about regulatory requirements on analytical methods, characterization of standards, impurities is needed.
• Experience in calibration and handling of different instruments like, HPLC, GC, UPLC, UV, IR, pH meter, Dissolution, Master Sizer, Zeta Sizer and KF titrator is required.
  
  

Required Educations, Skills, And Experience

• Masters in pharmacy and Masters in Chemistry
  
  

Physical & Mental Requirements

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

• Must be able to sit for long periods of time
• While performing the duties of this job, the employee is frequently required to stand; walk; sit; talk and/or hear
• May occasionally climb stairs and/or ride elevators
• The employee must occasionally lift and/or move up to 25 pounds
• Employee must be able to manipulate keyboard, operate a telephone and hand-held devices
• Other miscellaneous job duties as required