Assistant Qc Manager

Topgear Consultants; Nagpur District; On-site; INR 600,000 - 800,000; Full time

Job summary

Topgear Consultants in Nagpur district, Maharashtra, seeks an experienced QC Laboratory Manager to oversee day-to-day QC activities, allocate work to Chemists and Executives, and review chemical and microbiological testing results and documentation.

The role requires ensuring GMP/GLP/GDP compliance, preparing SOPs and formats, monitoring batch release status, handling change controls, training, inventory, and audit readiness, and coordinating with QC, R&D, Production and other departments to

Qualifications

• Pharma/API/Excipient/Chemical manufacturing exposure to Chemical QC and Microbiology QC.
• GMP documentation, audits, batch release and laboratory team handling.

Responsibilities

• Manage day-to-day QC laboratory activities and allocate work to Chemists/Executives.
• Review chemical and microbiological testing results, records, logbooks and documentation.
• Ensure compliance with GMP, GLP, GDP, SOPs and quality systems.
• Prepare/review SOPs, GTPs, formats, logbooks and QC documents.
• Monitor batch release status and coordinate with Production.
• Handle Change Controls, training, laboratory inventory and audit readiness.
• Supervise Microbiology activities, including media preparation, sterilization, microbial testing and related records.
• Coordinate with QC, R&D, Production and other departments.
• Support internal and external audits and ensure the laboratory remains inspection-ready.

Job description

Role & responsibilities

• Manage day-to-day QC laboratory activities and allocate work to Chemists/Executives.
• Review chemical and microbiological testing results, records, logbooks and documentation.
• Ensure compliance with GMP, GLP, GDP, SOPs and quality systems.
• Prepare/review SOPs, GTPs, formats, logbooks and QC documents.
• Monitor batch release status and coordinate with Production.
• Handle Change Controls, training, laboratory inventory and audit readiness.
• Supervise Microbiology activities, including media preparation, sterilization, microbial testing and related records.
• Coordinate with QC, R&D, Production and other departments.
• Support internal and external audits and ensure the laboratory remains inspection-ready.

Preferred candidate profile

Pharma/API/Excipient/Chemical manufacturing, preferably having exposure to both Chemical QC + Microbiology QC, GMP documentation, audits, batch release and laboratory team handling.