Role & responsibilities
Perform testing of raw materials, packaging materials, in-process samples, and finished products as per specifications and test methods.
Operate analytical instruments including HPLC, UV-Visible Spectrophotometer, FTIR, Dissolution Apparatus, and pH Meter.
Handle laboratory software such as Empower, Lab Solutions, CDS Software, LIMS, and Microsoft Excel for data acquisition, analysis, and reporting.
Prepare standard and sample solutions and perform assay, related substances, dissolution, and content uniformity testing.
Review chromatograms, analytical results, and laboratory records to ensure data accuracy and integrity.
Maintain instrument calibration, qualification, and preventive maintenance records.
Investigate OOS, OOT, and laboratory deviations in compliance with SOPs and GMP requirements.




Ensure compliance with GLP, GMP, data integrity, and regulatory guidelines.
Support method validation, method transfer, stability studies, and audit activities.
Coordinate with QA and Production for timely release of raw materials and finished products.

Preferred candidate profile
B.Pharm, M.Pharm, B.Sc., or M.Sc. in Chemistry or a related field.
26 years of experience in Pharmaceutical Quality Control.
Hands-on experience in HPLC operation, troubleshooting, and data review.
Robust knowledge of GMP, GLP, pharmacopoeial requirements, and laboratory documentation.

📌 Qc Analyst Paonta Sahib (India)
🏢 Mankind Pharma
📍 India