Executive - QC (Pharma)

ESP Engineered; India; On-site; INR 300,000 - 500,000; Full time

Job summary

ESP Engineered in India is looking for a candidate responsible for conducting proper laboratory analysis in compliance with the current product specifications and good manufacturing practices. The role involves extensive testing of raw materials and finished products, ensuring data accuracy and compliance with established procedures.

The ideal candidate will maintain lab standards, manage compliance, and handle changes and incidents within the laboratory operations, assuring quality in every process.

Responsibilities

• Ensure proper laboratory analysis as per MOA and current product specification.
• Testing of all raw material sample, stability samples and finished product samples.
• Responsible for Wet analysis, Instrument analysis & Purified Water analysis and NABL accreditation certificate.
• Ensure that the data generated is accurate, scientifically valid and compliant to the procedures.
• Maintain the lab work as per Current Good Manufacturing Practice standards (cGMP).
• To conduct sampling test as per Test Intimation sheet, fill up the sheet and attach supporting documents of testing and instrument report after completion of QC testing.
• Raise laboratory Change control, incidents, deviations and LI wherever applicable.
• To extract samples and pack the same for third party QC testing, send the sample along with specifications to the third-party testing lab.
• To maintain all record viz, consumption, Column, humidity, all instrument logbooks.
• Ensuring compliances to EHS policies, cGMP policies, data integrity policies and IT policies as per requirements.

Job description

Responsibilities

• Ensure proper laboratory analysis as per MOA and current product specification
• Testing of all raw material sample, stability samples and finished product samples
• Responsible for Wet analysis, Instrument analysis & Purified Water analysis and NABL accreditation certificate
• Ensure that the data generated is accurate, scientifically valid and compliant to the procedures.
• Maintain the lab work as per Current Good Manufacturing Practice standards (cGMP)
• To conduct sampling test as per Test Intimation sheet, fill up the sheet and attach supporting documents of testing and instrument report after completion of QC testing
• Raise laboratory Change control, incidents, deviations and LI wherever applicable
• To extract samples and pack the same for third party QC testing, send the sample along with specifications to the third-party testing lab
• To maintain all record viz, consumption, Column, humidity, all instrument logbooks
• Ensuring compliances to EHS policies, cGMP policies, data integrity policies and IT policies as per requirements

Skills

• Planning of analysis
• Working Standard Preparation and its evaluation with documentation.