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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