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Qc Analyst – Raw Material & Packaging Material (Rm/Pm Quality Control – Chemical Testing)

IPCA Laboratories Limited
0-3 years
Not Disclosed
Dhar, India
1 June 4, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: gmp knowledge, HSE Knowledge , Logistics and Transportation Management, Master Data, Operational Excellence, Sap Erp, supply chain management, Supply Planning, Warehouse Management, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing

QC ANALYST – RAW MATERIAL & PACKAGING MATERIAL (RM/PM QUALITY CONTROL – CHEMICAL TESTING)

JOB SUMMARY
A Quality Control (QC) Analyst – RM/PM role responsible for testing raw materials, packaging materials, and utilities in a GMP-regulated pharmaceutical environment. The role involves chemical analysis, instrumental testing, and ensuring material compliance with pharmacopeial and internal quality standards before release into manufacturing processes.

EXPERIENCE REQUIRED
Fresher to 3 years of experience in Quality Control, chemical analysis, or pharmaceutical laboratory testing. Fresh graduates with strong chemistry lab exposure may also apply.

EDUCATION QUALIFICATION
M.Sc / M.Tech / B.Tech in Chemistry or related chemical science discipline.

KEY RESPONSIBILITIES

  • Perform raw material (RM) and packaging material (PM) testing as per approved specifications

  • Conduct chemical analysis using techniques such as Karl Fischer (KF), FTIR, and titration methods

  • Carry out water testing and gas sampling analysis as per GMP requirements

  • Operate and maintain laboratory instruments including coulometer, auto titrator, and related analytical equipment

  • Ensure proper sampling, labeling, and testing of incoming materials

  • Maintain accurate documentation of all test results in compliance with GMP/GLP guidelines

  • Support calibration, verification, and routine maintenance of QC instruments

  • Ensure adherence to SOPs, pharmacopeial standards, and data integrity requirements

  • Assist in investigation of deviations, OOS (Out of Specification) results, and quality incidents

KEY SKILLS REQUIRED

  • Strong foundation in organic and inorganic chemistry concepts

  • Hands-on experience with QC laboratory instruments and wet chemistry techniques

  • Understanding of GMP, GLP, and pharmaceutical quality systems

  • Strong documentation, reporting, and data integrity practices

  • Attention to detail and ability to work in regulated environments

  • Basic troubleshooting skills for analytical instruments