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Formulation Chemist

SAIN MEDICAMENTS PVT. LTD
Full Timemid
Telangana, INPosted April 25, 2026

Job Description

Job Title: Chemist – Liquid Manufacturing

Industry: Pharmaceuticals (Formulation – Manufacturing)

Department: Production

Job Summary

We are looking for a dedicated Liquid Manufacturing Chemist to manage and execute the manufacturing of liquid oral formulations in a GMP-compliant facility. The role involves batch processing, documentation, process monitoring, and ensuring adherence to quality and regulatory standards.

Key Responsibilities:

  • Execute manufacturing of liquid formulations (syrups, suspensions, solutions) as per BMR and SOPs
  • Dispensing and verification of raw materials as per approved procedures
  • Operate and monitor manufacturing equipment such as reactors, mixing vessels, and transfer systems
  • Ensure proper batch processing parameters (temperature, mixing time, pH, etc.) are maintained
  • Maintain accurate Batch Manufacturing Records (BMR) and logbooks in real-time
  • Perform in-process checks and coordinate with QA/QC for sampling and approvals
  • Ensure cleaning and sanitization of equipment as per SOPs
  • Follow GMP, safety, and hygiene practices strictly
  • Report deviations, incidents, or abnormalities during manufacturing
  • Support scale-up, validation, and process improvement activities

GMP & Compliance Responsibilities:

  • Adhere to GMP guidelines and data integrity practices
  • Ensure audit readiness at all times
  • Participate in internal and external audits
  • Maintain documentation as per regulatory requirements

Key Skills:

  • Liquid Manufacturing (Orals)
  • GMP / SOP Compliance
  • BMR Documentation
  • Process Monitoring & Control
  • Equipment Handling (Reactors, Mixing Tanks)
  • Pharma Production

Eligibility Criteria:

  • Qualification: B.Pharm / M.Pharm / B.Sc / M.Sc (Chemistry)
  • Experience: 8–10 years in pharmaceutical liquid manufacturing

Preferred Candidate Profile:

  • Experience in GMP-approved formulation units
  • Knowledge of regulatory requirements (WHO, USFDA, etc.)
  • Good understanding of audit processes
  • Strong attention to detail and documentation

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