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Senior Executive - Quality Assurance

AzurityOnsite
This job is no longer open

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.

Principle Responsibilities:


  • Responsible for review of batch documentation received from the contractor site.
  • Preparation and verification of the APQR for the executed batches.
  • Responsible for review of the process validation protocols and reports.
  • Ensures all GMP’s, SOPs, and protocols are followed during the batch execution.
  • Review and certification of protocols related to CMC- dossier submission.
  • Positively interacts with internal associates, contractors, and partners to resolve issues quickly and effectively.
  • Support in implementation of CAPAs, Quality improvement initiatives, and other QMS activities.
  • Preparation of the standard operating procedures related to Quality Assurance.

Qualifications and Education Requirements:


  • Post-graduate in pharmacy with a good academic background.
  • Industrial experience: 3-5 years in a reputed pharmaceutical organization with exposure in IPQA preferably in sterile manufacturing operations.

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


This job is no longer open

Life at Azurity

Azurity’s mission is to make safe, high-quality treatments for patients who require formulations of drugs other than what is commonly commercially available (such as tablets and capsules).
Thrive Here & What We Value1. Inclusive Workplace2. Equal Opportunity Employer3. Patient-centric Products4. Innovative, High-quality Products for Underserved Patients5. Collaborative and Respectful Relationships with Partners6. Commitment to Quality in Everything Done7. Dedicated Team Focused on Benefiting Lives of Patients8. Private Equity Backed High-Growth Company9. Broad Commercial Product Portfolio and Robust Late-Stage Pipeline10. Talented, Incredible Team with a Passion for Science and Quality
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