Core Testing &
Analysis
Sample Testing: Analyze raw materials, in-process mixtures, final small-volume injections, and stability study samples.
Solution Preparation: Make mobile phases, standard references, blanks, and test samples accurately.
Method Execution: Follow pharmacopeial guidelines like IP, USP, or BP alongside exact in-house protocols.

Instrument Operation &
Care
Daily Operation: Run, monitor, and shut down HPLC systems for assays and impurity tests.
Calibration &
Tuning:

Perform system suitability tests, routine calibrations, and performance checks before testing.
Troubleshooting: Fix common HPLC issues like baseline noise, pressure spikes, leaks, or pump errors.

Compliance &
Data Integrity
Documentation: Record all calculations, weight logs, and sequence runs following Positive Laboratory Practices (GLP) and Valuable Documentation Practices (GDP).
Data Security:



Ensure electronic data and audit trails comply with 21 CFR Part 11 and ALCOA+ principles.
Deviation Management: Report and document Out of Specification (OOS) or Out of Trend (OOT) results immediately.

Audit &
Team Support
Cross-Functional Work: Share timely batch release data with the Production and Quality Assurance (QA) teams.
Audit Readiness: Help manage documentation and answer questions during internal reviews and external regulatory inspections (USFDA, WHO, MHRA).

Pay: ₹30,000.00 - ₹45,000.00 per month

Perks
Flexible schedule
Food provided
Health insurance
Leave encashment
Life insurance
Paid sick time

Education
Bachelor's (Required)

Experience
Qc Hplc: 4 years (Required)

Work Location: In person

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