QC - L 6 To L 7

About the role

To perform quality control testing and analysis of raw materials, finished products, stability samples, and microbiological parameters as per current Good Manufacturing Practices (cGMP), standard operating procedures (SOPs), pharmacopeial standards, and regulatory requirements to ensure product quality and compliance.

What you'll do

• Perform chemical and instrumental testing of Raw Materials (RM) and Finished Goods (FG) as per pharmacopeial and in-house specifications
• Conduct Stability Studies in line with ICH guidelines and maintain records of stability trends
• Execute Analytical Method Validations (AMV) and support Process Validation (PV) testing
• Carry out Microbiological analysis of samples, including environmental monitoring, water testing, and microbial limit tests
• Maintain accurate, complete, and timely documentation (analytical reports, logbooks, LIMS/ERP entries)

What you need

• 2–5 yrs of experience
• GMP
• Microbiology
• Chemistry
• Preventive maintenance
• SOP writing
• GLP
• M.Sc or B.Pharm or M.Pharm

Good to have

• ISO 9001
• ERP
• Internal audit
• HPLC
• Regulatory affairs

What you get

• ₹6 L–₹7 L a year