Quality Analyst

Entirety Hr Solutions; Telangana; On-site; INR 350,000 - 520,000; Full time

Job summary

Entirety Hr Solutions in Telangana, India handles calibration and maintenance of HPLC, GC and related laboratory instruments, and prepares and standardizes volumetric solutions and reagents.

You will perform analysis of raw materials, in-process samples, intermediates and finished products, conduct method validation and transfers, maintain QC records, review documents, and ensure GMP/GLP and SOP compliance with QA coordination.

Qualifications

• Calibration and maintenance of HPLC and GC instruments.
• Preparation and standardization of volumetric solutions and reagents.
• Familiarity with GMP, GLP and SOP requirements.

Responsibilities

• Perform calibration and maintenance of HPLC and GC instruments.
• Analyze raw materials, in-process samples, intermediates and finished products.
• Conduct method validation, method transfer and cleaning verification activities.
• Maintain QC documentation and calibration logs; coordinate with QA for records.

Skills

HPLC

GC

Calibration

Method validation

Documentation

GMP/GLP/SOPs

Job description

QC Instrumentation Analyst and QC Wet Analyst

• Handle calibration and maintenance of HPLC, GC, and other laboratory instruments as per SOPs.
• Prepare and standardize volumetric solutions, reagents, and maintain related records.
• Perform analysis of raw materials, water, in-process samples, intermediates, finished products, packaging materials, stability, and hold-time samples.
• Conduct sampling, method validation, method transfer, and cleaning verification activities.
• Maintain analytical records, calibration logs, stability studies, and QC documentation.
• Review executed documents and coordinate with QA for documentation handover.
• Ensure laboratory housekeeping, temperature monitoring, and compliance with GMP, GLP, and SOP requirements.

• Perform calibration of wet laboratory instruments and maintain calibration records.
• Prepare and standardize volumetric solutions, reagents, and maintain documentation.
• Conduct wet chemical analysis of raw materials, water, in-process samples, intermediates, finished products, packaging materials, and stability samples.
• Perform sampling of raw materials, packaging materials, intermediates, and finished products.
• Execute method transfer and UV cleaning verification activities.
• Maintain QC records, stability studies, and quality documentation.
• Review QC documents and hand over completed records to QA while ensuring laboratory cleanliness and compliance with GMP, GLP, and SOPs.