Executive / Sr Executive -Quality Control

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Job Summary:

We are looking for dynamic and detail-oriented professionals to join our Quality Control – Formulation team. The role involves analysis and testing of raw materials, in-process samples, finished products, and stability samples, ensuring compliance with cGMP and regulatory requirements.

Key Responsibilities:

• Conduct routine analysis of raw materials, in-process, finished products, and stability samples as per approved specifications and procedures.
  
• Perform analysis using analytical instruments such as

  HPLC, GC, UV-Vis Spectrophotometer, FTIR, Dissolution Tester, etc.

• Prepare and review analytical reports, protocols, and standard operating procedures (SOPs).
  
• Ensure all laboratory activities comply with

  cGMP, GLP, and regulatory standards

  (USFDA, EU, WHO, etc.).
• Maintain and calibrate laboratory instruments and ensure proper documentation.
  
• Handle Out of Specification (OOS), Out of Trend (OOT), and deviation investigations.
  
• Coordinate with cross-functional teams such as QA, Production, and R&D for smooth workflow.
  
• Participate in regulatory and internal audits, and support audit readiness of the QC lab.
  
• Maintain records and documents as per Data Integrity and ALCOA+ principles.
  

Candidate Requirements:

• Qualification:

  B.Pharm / M.Pharm / M.Sc in Chemistry / Pharmaceutical Sciences

• Experience:

  1–7 years in Quality Control (Formulation) in a pharmaceutical company.
• Hands-on experience with

  analytical instruments

  (especially HPLC, GC).
• Knowledge of

  ICH guidelines

  , cGMP, and regulatory norms.
• Good documentation practices and exposure to

  analytical method validation

  is preferred.
• Proficient in MS Office and LIMS (Laboratory Information Management System) is a plus.
  
• Strong analytical thinking, communication skills, and team collaboration.
  

Best Regards

Team Jodas Expoim