Job Description

Job Summary:

We are seeking a skilled and detail-oriented

QC Analyst

with hands-on experience in

HPLC (High-Performance Liquid Chromatography) and GC (Gas Chromatography)

for our chemical manufacturing operations. The ideal candidate will be responsible for performing routine and non-routine analysis of raw materials, in-process samples, and finished products to ensure compliance with quality standards and regulatory requirements.

Key Responsibilities:

Perform qualitative and quantitative analysis of chemicals using

HPLC, GC, and other analytical instruments

. Conduct method development, validation, and optimization for analytical testing as required. Prepare and maintain

accurate laboratory records, SOPs, and test reports

in compliance with cGMP and company standards. Troubleshoot instrument issues, perform routine maintenance, and ensure calibration of laboratory equipment. Analyze deviations, non-conformances, and contribute to root cause analysis for QC failures. Collaborate with production, R&D, and QA teams to support product quality and process improvement initiatives. Ensure compliance with

safety, environmental, and regulatory requirements

.

Required Qualifications & Skills:

Bachelor's or Master's degree in

Chemistry, Pharmaceutical Sciences, Biochemistry, or related field

.

3-8 years of hands-on experience

in QC labs of chemical, pharmaceutical, or related industries. Proficient in

HPLC and GC techniques

; experience with other analytical techniques (UV, FTIR, Titration) is a plus. Knowledge of

analytical method validation, SOPs, GLP, and cGMP practices

. Strong

data interpretation and troubleshooting skills

. Excellent documentation skills and attention to detail. Familiarity with

laboratory safety practices and chemical handling protocols

.
Job Types: Full-time, Permanent

Pay: ?300,000.00 - ?600,000.00 per year

Benefits:

Food provided Health insurance Paid sick time Paid time off Provident Fund
Work Location: In person