QA Pharma Job Opening

QA Pharma Job Opening at Apotex – Apply Online Now

Executive, Quality Assurance-ARPL-AQAR AR

Date: May 31, 2024

Location: Bangalore, KA, IN, 560099

Company: Apotex

About Apotex Inc.
Apotex Inc. is a Canadian-based global health company that produces high-quality, affordable medicines for patients around the world. Apotex employs almost 7,200 people worldwide in manufacturing, R&D, and commercial operations. Apotex medicines are accessible to patients in more than 75 countries globally. Through vertical integration, the Apotex group is focused on the development and sale of generic, biosimilar, and specialty products. For more information visit:

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

Job Responsibilities

  • Responsible for Successful Health Authority inspection.
  • Responsible to review analytical documents like Commercial stability, IP, SFG, RM, PM.
  • Responsible to review qualification reports for laboratory instruments.
  • Responsible to review calibration reports for laboratory instruments.
  • Responsible to review working standard reports.
  • Review of analytical documents generated by laboratories.
  • Responsible to review Deviations, Lab events, Temporary Changes, CAPAs, Non-CAPA Follow-up tasks, and LIRs.
  • Responsible to review/verification of analytical data through LIMS.
  • Responsible for completion of training prior to execution of any activity.
  • Documentation control: Responsible for submitting the documents for archival and updating documentation as per SOP.
  • To provide, execute and impart training with respect to procedures review and updation.
  • To be responsible for all activities in 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 Behaviors 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.

Job Requirements


Minimum Bachelor of Pharmacy/Science or any equivalent degree

Knowledge, Skills, and Abilities

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


Minimum 2 years of experience in a GMP regulated industry

Link to apply: APPLY ONLINE HERE

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