59 Job openings found

Position:          QC Executive Location:          Silvassa  Experience:      6 - 10  Years Industries:       Pharma   Responsibilities: Analytical Testing: Perform routine and non-routine analysis of raw materials, in-process samples, finished products, and stability samples using HPLC, GC, UV, IR, etc. Conduct assay, dissolution, impurity profiling, and related substance testing as per pharmacopeial standards (USP, BP, IP, etc.). Instrument Operation & ...

Job Description : 26/03/2024   HPS/2024/173 Qc executive Male 1 0 to 2 DME/B.Tech Qc executive for Plastic sheet line :  We need a guy who should manage quality control of incoming raw material, packing material, online qc inspection on the production line, Qc of finished goods, Qc reports and documentation. Should know about all about ISO. HPLC (Operation and ...

Experience/Technical Skills :   Should have work experience in ADL Lab /PD Lab Should be aware about Method Development and Method Validation Should have knowledge of HPLC and GC Should have knowledge and Work experience in ADL/R&D /PD Lab for analytical exposure Should have ability to draft/prepare specification from monograph Knowledge of ICH will be more appreciated

Experience/Technical Skills :   Should have work experience in ADL Lab /PD Lab Should be aware about Method Development and Method Validation Should have knowledge of HPLC and GC Should have knowledge and Work experience in ADL/R&D /PD Lab for analytical exposure Should have ability to draft/prepare specification from monograph Knowledge of ICH will be more appreciated

Job Description:1. Analysis1.1  Raw material / packing material analysis at the time of incoming1.2  In process analysis time to time1.3  Finished product analysis and compare to require specification compliance2. Manage QC lab2.1  Method validation – Set test methods as pharmacopoeia and GMP requirement.2.2  Instrument calibration: Prepare calibration Schedule and calibration ...

Job Description:1. Analysis1.1  Raw material / packing material analysis at the time of incoming1.2  In process analysis time to time1.3  Finished product analysis and compare to require specification compliance2. Manage QC lab2.1  Method validation – Set test methods as pharmacopoeia and GMP requirement.2.2  Instrument calibration: Prepare calibration Schedule and calibration ...

Job Description:1. Analysis1.1  Raw material / packing material analysis at the time of incoming1.2  In process analysis time to time1.3  Finished product analysis and compare to require specification compliance2. Manage QC lab2.1  Method validation – Set test methods as pharmacopoeia and GMP requirement.2.2  Instrument calibration: Prepare calibration Schedule and calibration ...

Bulk & Finished Products analysis by UV-VIS Spectrophotometer. Prepare Analysis Report of Bulk Products. Prepare COA of Finished Products. Raw Material analysis. Calibration of Ultraviolet Calibration of pH meter. Operate HPLC. Calibration of HPLC. Responsible For all Activity of Q.C Department ,cGLP as per 21(CFR)part 11,DRA documents for export, Ensure and review,Approval of R.M Finished Products and Stability of ...

A Sr. Chemist QC (Quality Control) analyzes raw materials, in-process samples, and finished products using advanced techniques (HPLC, GC) to ensure quality, consistency, and regulatory compliance (GMP, ISO), requiring strong analytical skills, documentation, equipment management, and leadership to mentor junior staff and resolve complex quality issues. Key duties involve developing SOPs, ...

Position:      QC Officer Location:       Dahej Experience:    3 - 4 Years Industries:     Pharma API  Responsibilities: Perform chemical and physical analysis of raw materials, in-process samples, and finished products as per approved specifications. Ensure testing is carried out in compliance with SOPs, GMP, and safety guidelines. Maintain accurate laboratory records, test reports, and logbooks. Calibrate, ...