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⏰ Full-time

Officer - Quality Control

Centrient Pharmaceuticals
Location 📍 Rupnagar, India
Posted 📅 June 06, 2026
Work Type ⏰ Full-time

Position Overview

Description

Position Description :

Position ensures that the products provided to the market are tested as per customer specifications and in compliance with applicable pharmacopoeias as well cGMP/GLP/ICH/USFDA/ISO guidelines.

Key Responsibilities:

  • Analysis of Finished products / raw materials/ in process & stability samples (Wet & Instrumental analysis).
  • Preparing stability trend and then sharing with all stake holders.
  • Conducting LSC to update all stake holders on stability status.
  • Calibration of HPLCs as per defined procedure and schedule.
  • Method validations as per applicable guidelines.
  • Inventory management of reagents/columns spares etc. required for Premix analysis.
  • Mobile phase preparation and their record keeping.
  • Printing and preparation of record of analysis.
  • Log books management for various activities.
  • Preparation/Revision of method of an...
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    Job Details

    Employment Type
    Full-time
    📊
    Category
    Other Production Occupations
    🏠
    Work Arrangement
    On-site
    📍
    Location
    Rupnagar, India