Analyst - QC

Name of the Company – Zydus Healthcare Limited

Industry – Pharmaceuticals

Website of the company - https://www.zyduslife.com/zyduslife/

Location –Sikkim Unit I & Unit II

Position - Officer / Executive

Qualification – M.Sc. / B.Sc. in Chemistry, Microbiology & Biotechnology

Experience Required – Between 1 to 4 Years Of Experience

Role – QC Analyst

No’s of Vacancy - 5

Key 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.

Required Skills

• 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 [email protected]

Job Snapshot

Updated Date

09-10-2026

Job ID

JOB11177

Department

SIKKIM QC

Location

Zhl - Sikkim|zhl-sikkim Plt., Gangtok, Sikkim, India ..+ 1

Experience

1 - 4 Years

Employee Type

P-P7-Probationer-HO Staff