44 Job openings found

Key Responsibilities: Perform analysis of raw materials, in-process samples and finished products. Handle routine QC testing as per approved specifications and SOPs. Operate and maintain laboratory instruments and equipment. Prepare and maintain analytical reports, worksheets and QC documentation. Follow GLP, GMP and safety procedures. Support method validation, calibration and stability-related activities. Ensure proper sampling, testing and documentation ...

Key Responsibilities: Perform analysis of raw materials, in-process samples and finished products. Handle routine QC testing as per approved specifications and SOPs. Operate and maintain laboratory instruments and equipment. Prepare and maintain analytical reports, worksheets and QC documentation. Follow GLP, GMP and safety procedures. Support method validation, calibration and stability-related activities. Ensure proper sampling, testing and documentation ...

  Analytical Method Development: Develop, optimize, and troubleshoot analytical methods for assay, dissolution, related substances/impurities, and residual solvents. Method Validation: Execute analytical method validation as per ICH guidelines, including accuracy, precision, specificity, linearity, range, robustness, and system suitability. Instrument Operation: Hands-on experience with HPLC, GC, UV-Vis, FTIR, and Karl Fischer titrators, including instrument ...

  Perform routine quality control analysis of raw materials, packing materials, in-process and finished products. Operate and maintain HPLC and GC instruments for analytical testing. Perform sample preparation, testing and documentation as per approved SOPs and specifications. Review analytical results and ensure compliance with specifications. Maintain proper laboratory records, logbooks and analytical worksheets. Follow GMP, GLP ...

Key Responsibilities:Perform analysis of raw materials, intermediates, finished products, and packing materials as per approved specifications.Conduct routine chemical testing and maintain accurate laboratory records.Operate and maintain laboratory instruments such as GC, HPLC, UV Spectrophotometer, Karl Fischer, pH Meter, and other analytical equipment.Prepare and standardize chemical reagents, solutions, and volumetric preparations.Ensure ...

Key Highlights Department: Health, Safety, Environment & Quality (HSEQ) Reporting To: Assistant Manager – QA/QC Experience Required: 4–6 Years Qualification: B.Sc in Quality or Engineering Core Responsibilities: Laboratory analysis of raw materials, finished goods & waste samples Calibration & troubleshooting of analytical instruments Documentation as per ISO 9001 standards SOP, checklist & compliance management In-process & finished product analysis Inventory management ...

🔬 Quality Testing & Analysis Perform routine and non-routine chemical analyses on raw materials, in-process samples, and finished goods using standard laboratory methods. Operate and validate analytical instruments such as HPLC, GC, UV-Vis, FT-IR, Karl Fischer titrator and other relevant equipment. Record, calculate, interpret and report accurate analytical results, ensuring data integrity and ...

🔬 Quality Testing & Analysis Perform routine and non-routine chemical analyses on raw materials, in-process samples, and finished goods using standard laboratory methods. Operate and validate analytical instruments such as HPLC, GC, UV-Vis, FT-IR, Karl Fischer titrator and other relevant equipment. Record, calculate, interpret and report accurate analytical results, ensuring data integrity and ...

🔬 Job Responsibilities ✔ Quality testing of Raw Materials, Intermediates & Finished Goods ✔ Sampling as per guidelines ✔ Testing as per specifications & SOPs ✔ Recording & analyzing test data ✔ Preparation & verification of standard solutions ✔ Calibration & verification of lab instruments (pH meter, conductivity meter, balance, etc.) ...

🔑 Key Responsibilities GMP Compliance Ensure effective implementation of GMP guidelines across production, QA, QC, warehouse, and utilities. Monitor day-to-day GMP activities and identify non-conformances. Support GMP audits (internal, customer, and regulatory). Documentation & Records Prepare, review, and control GMP documents such as SOPs, formats, logs, and registers. Ensure proper documentation practices (GDP) are followed. Maintain training, deviation, ...