Analyst - QC

Responsibilities

• Perform analysis of Raw Materials (RM), Finished Products (FP), Stability Samples, Water Samples, and Microbiological Samples as per approved specifications and test methods.
• Conduct testing using HPLC, GC, UV-Visible Spectrophotometer, FTIR, Dissolution, and other analytical instruments.
• Perform microbiological testing including Environmental Monitoring, Water Testing, Bioburden, and Microbial Limit Testing.
• Monitor stability studies and perform testing as per approved stability protocols and ICH guidelines.
• Prepare and standardize reagents, volumetric solutions, culture media, and reference standards.
• Review analytical and microbiological data and ensure compliance with established specifications.
• Maintain laboratory records, logbooks, worksheets, analytical reports, and documentation as per GMP and GLP requirements.
• Investigate OOS, OOT, laboratory incidents, and microbiological deviations.
• Ensure compliance with GMP, GLP, Data Integrity, and Safety requirements.
• Support method validation, method transfer, instrument qualification, and calibration activities.
• Participate in internal audits, regulatory inspections, and compliance-related activities.
• Coordinate with QA, Production, Engineering, and Regulatory Affairs for laboratory-related activities.
• Ensure proper maintenance, calibration, and operation of laboratory instruments and equipment.

Requirements

• Name of the Company – Zydus Healthcare Limited
• Industry – Pharmaceuticals
• Website of the company -
• Location –Sikkim Unit I & Unit II
• Position - Officer / Executive
• Qualification –. in Chemistry, Microbiology & Biotechnology
• Experience Required – Between 1 to 4 Years Of Experience
• Role – QC Analyst

No’s of Vacancy - 5

• Hands-on experience with HPLC, GC, UV, FTIR, Dissolution, and other analytical instruments.
• Knowledge of microbiological testing, Environmental Monitoring, and Water Analysis.
• Understanding of GMP, GLP, Data Integrity, and laboratory compliance requirements.
• Knowledge of pharmacopeial requirements including IP, USP, BP, and EP.
• Familiarity with OOS, OOT, CAPA, Deviation, Change Control, and QMS processes.
• Strong analytical, troubleshooting, documentation, and communication skills.
• Proficiency in laboratory documentation and data review practices.

Preferred

• Experience Experience in pharmaceutical Quality Control laboratories handling RM, FP, Stability, and Microbiology activities.
• Exposure to regulatory audits and GMP-compliant laboratory operations.
• Experience in analytical method validation, stability studies, and microbiological testing.
• Knowledge of laboratory software, chromatography data systems, and electronic documentation practices.
• Hands-on experience with regulated manufacturing environments and quality systems.
• Interested candidates may share their CV at