Job Requirements: 

• Msc, Mtech, & BE, Chemical Engineering, industrial Chemistry or a related field. Advanced degree or certification in Quality Assurance or Quality Control is a plus. 

• Minimum 2-4 years of experience in quality assurance and quality control within the chemical manufacturing industry. 

• Proven experience with quality management systems (e.g., ISO 9001, ATMS, GMP). 

• Proficiency in sample preparation, calibration, and molarity calculation. 

• Understanding of QA & QC standards and practices. 

• Expertise in data collection, interpretation, and analysis. Experience in preparing accurate documentation and technical reports. 

• Ability to troubleshoot technical issues and perform routine equipment maintenance. 

• Effective communication skills and the ability to work collaboratively within a team. 

Job Responsibilities: 
 

1.Analytical Testing: 

• Operate and maintain ICP-OES (Inductively Coupled Plasma Optical Emission Spectroscopy), ICP-MS (Inductively Coupled Plasma Mass Spectrometry), UV-Vis (Ultraviolet-Visible Spectroscopy), XRD (X-ray Diffraction), and FTIR (Fourier Transform Infrared Spectroscopy) instruments. 

• Perform routine and specialized analyses to support quality control and assurance efforts. 

2.Sample Preparation & Instrument Calibration: 

• Prepare samples for analysis, including digestion, dilution, and other necessary treatments. 

• Ensure samples are processed following established protocols to maintain accuracy and integrity. 

• Calibrate analytical instruments regularly to ensure accurate measurements. 

• Calculate molarity and prepare standard solutions for use in various analytical methods. 

3.Data Collection and Interpretation: 

• Collect, record, and analyse data from analytical tests with precision. 

• Interpret results to ensure they meet established quality standards and specifications. 

• Identify and troubleshoot any data anomalies or inconsistencies. 

4.Quality Assurance & Quality Control: 

• Follow QA QC procedures to maintain the accuracy and reliability of test results. 

• Participate in internal and external audits to verify compliance with quality standards. 

• Assist in developing and refining QA QC procedures and practices. 

5.Documentation and Reporting: 

• Maintain detailed and accurate records of testing activities, results, and calibrations. 

• Prepare technical reports and documentation related to QA & QC activities. 

• Communicate findings and recommendations to relevant stakeholders. 

6.Equipment Maintenance: 

• Perform routine maintenance and calibration of laboratory equipment. 

• Report and address any issues or malfunctions with analytical instruments. 

7.Collaboration and Communication: 

• Work closely with R&D scientists, engineers, and project managers to address quality-related concerns and drive improvements. 

• Participate in project meetings and provide insights on quality-related issues and solutions. 

• Act as a liaison between the R&D department and other departments (e.g., Manufacturing, Regulatory Affairs) to ensure alignment on quality objectives. 

8.Continuous Improvement: 

• Contribute to efforts aimed at improving laboratory processes, quality control procedures, and analytical techniques. 

• Stay informed about advancements in analytical technologies and QA & QC practices.