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  • To Monitor, interpret and apply international regulatory guidelines (e.g., WHO GMP, PIC/S GMP, EMA regulations, TGA requirements, ICH guidelines) to internal documentation and processes.
  • Conduct gap‐analyses of current documentation/SOPs against the latest regulatory requirements and update as needed.
  • Develop, revise and maintain SOPs (Standard Operating Procedures), policies, work instructions and regulatory documentation to ensure compliance with global regulatory requirements.
  • Coordinate with cross-functional departments (Quality Assurance, Manufacturing, R&D, Regulatory Affairs, Supply Chain) to collect data and documentation, ensure changes in regulations are incorporated into documentation.

Job Type: Full-time

Pay: Rs70,000.00 - Rs95,000.00 per month

Work Location: In person

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