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CPPL / Career

Working @ChemoxPharma

At Chemox Pharma, our team members are our most important assets and are the reason for our continued success. We value ideas and give our people the space to execute them. We are always looking for talented individuals who would like to become part of our team.

We keep our people intellectually motivated and empower them to make their own decisions, helping CPPL grow together through innovation and execution.

Chemist – Production

Experience: 2–4 years (API Pharma)
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Chemist – Production

Job Description

  • Requisition, receive, and verify raw materials as per batch requirements.
  • Perform batch operations, charging, and utility operations.
  • Maintain Batch Manufacturing Records, Batch Packing Records, and Equipment Cleaning Records.
  • Operate all plant equipment as per SOPs and verify equipment status before use.
  • Coordinate with QC for in-process and finished product testing.
  • Liaise with Engineering for equipment calibration, AMC, and preventive maintenance.
  • Ensure compliance with health, safety, and environmental regulations.
  • Prevent spillage, contamination, and ensure proper labelling after batch completion.
  • Participate in investigations and report discrepancies to the Production Manager.
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Warehouse Officer

Experience: 2-4 Years
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Warehouse Officer

Job Description

  • Maintain receipt and dispensing of raw materials and packing materials.
  • Update daily stock registers and bin cards.
  • Prepare stock statements.
  • Ensure cleaning, arrangement, and status labelling in packing material stores.
  • Maintain humidity control, cleaning, and calibration.
  • Handle materials properly and ensure safe storage of RM/PM.
  • Receive and dispense materials as per GMP procedures.
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QA Officer

Experience: 2-4 years
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QA Officer

Job Description

  • Prepare and implement quality assurance policies and procedures.
  • Ensure compliance with standards, quality policy, and safety regulations.
  • Prepare, review, issue, distribute, and archive GMP documents for finished product manufacturing.
  • Review and release raw materials, packing materials, intermediates, and finished products.
  • Review BMR, BPR, ECR, and analytical raw data for product approval.
  • Monitor cleanliness and labelling of finished product containers.
  • Review and approve OOS, deviations, non-conformances, and investigations.
  • Ensure all operations are performed according to SOPs and GMP requirements.
  • Review and approve SOPs, protocols, and reports.
  • Conduct and coordinate GMP training sessions.
  • Inspect manufacturing activities to maintain QA standards.
  • Manage the Quality Management System for continuous improvement.
  • Verify effectiveness of corrective and preventive actions (CAPA).
  • Perform internal and external audits.
  • Coordinate with Production, QC, Facilities, Materials Management, Accounts, Purchase, and Warehouse for quality compliance.
  • Oversee dispatch activities and monitor housekeeping in all departments.
  • Perform any additional duties as assigned.
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