Executive, Quality Assuranc-ARPL-AQAR AR

Responsible for Review of Analytical Documents (Stability Reports/SFG/IP/FP/RM/PM).

• Responsible for Successful Health Authority inspection.


• Responsible to review of analytical documents like Commerical stability, IP,SFG,RM,PM.


• Responsible to review of qualification reports for laboratory instruments.


• Responsible to review of calibration reports for laboratory instruments.


• Responsible to review of working standard reports.


• Review of analytical documents generated by laboratories.


• Responsible to review of Deviations, Lab event, Temporary Changes, CAPA s, Non CAPA Follow-up task and LIR s.


• Responsible to review/verification of analytical data through LIMS.


• Responsible for completion of training prior to execution of any activity.


• Documentation control: Resposnible for submitting the documents for archival and updation of documentation as per SOP.


• To provide, execute and impart training with respect to procedures review and updation.


• To be responsible for all activities in the Quality Assurance, including cGMP/ cGLP/ cGXP, documentation and implementation of departmental quality systems.


• Works in a safe manner collaborating as a team member to achieve all outcomes.


• Demonstrate Behaviours that exhibit our organizational Values: Collaboration, Courage, Perseverance, and Passion.


• Ensure personal adherence with all compliance programs including the Global Business Ethics and Compliance Program, Global Quality policies and procedures, Safety and Environment policies, and HR policies.


• All other duties as assigned.

• Education

  
  
  • Minimum Bachelor of Pharmacy/ Science or any equivalent degree
  
  
  
  



• Knowledge, Skills and Abilities

  
  
  • Good knowledge in day to day pharma updation
  
  
  • Good Management qualities
  
  
  • Vigilance at work
  
  
  
  



• Experience

  
  
  • Minimum 2 years of experience in GMP Regulated industry