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:
Our Administration team at Azurity Pharmaceuticals always strive for the excellence in all the facilities that were being provided for the Employees. We always look for dynamic personnel who bring a change in the approach and contribute to organizational excellence. The team has diversified responsibilities like lab administration & management, Procurement, EHS & Indian Licensing.
Principle Responsibilities:
This should specifically outline, in bullet form, the responsibilities of the job:
Licensing activities –
- Preparation and uploading of a suitable application for test license, NOC, Import Licenses as per the guidance of CDSCO & DCA.
- Preparing and applying in a suitable application for Narcotics/ control substance for Import licenses / No Objection Certificates from CBN, Gwalior.
- Securing support documents from the respective formulation team for the preparation of applications.
- Coordination with respective regulatory authorities and query response.
Stability Activities –
- Stability chambers management like continuous monitoring of chamber performance & maintenance including period qualifications.
- Stability Protocol execution like loading and unloading samples of in coordination with formulation team.
- Stability chamber data review and Alarm acknowledgment on day to day basis as per the SOP
- Documents management of related activities.
General Activities –
- Ensure completion of the required training courses and perform only those activities for which training has been completed, where required.
- Planning day-to-day activities and coordinating with interrelated departments.
Qualifications and Education Requirements –
- This section should include relevant qualifications and education requirements.
- 8 to 10+ years of experience as a Working Professional in a similar field.
- Shall hold any bachelor’s or Master’s degree relating to Pharmaceutical / life sciences
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
