Quality Assurance Manager

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 and batch disposition.
• Preparation and review of standard operating procedures related to Quality Assurance and review of SOP related to other cross functional teams.
• Review and approval of the QMS documentation such as change controls, deviations, and investigation, CAPA.
• Well versed in the review and approval of the APQR, process validation protocols and reports, protocols related to CMC- dossier submission and artworks of products.
• Positively interacts with internal stakeholders and external stakeholders such as contract manufacturing site/ contract testing labs.
• Support in implementation of CAPAs, Quality improvement initiatives, and other QMS activities.
• Ensuring qualifications of contractors, vendor through vendor questionnaire, audits, and quality agreement.
  
  

Qualifications And Education Requirements

• M. Pharm or B. Pharm with a good academic background.
• Industrial experience:8-10 years in a reputed pharmaceutical organization with exposure in IPQA preferably in oral solid manufacturing operations.
  
  

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.