This role requires a strong background in analytical chemistry and a hands-on experience with HPLC instrumentation, along with both technical skills and soft skills like problem-solving, communication, and collaboration with team management. Key Responsibilities: Planning of samples for HPLC, team and shift management , checking and confirmation of all technical data in QC , Report delivery and monitoring of team for technical details. Developing and validating HPLC methods for impurity analysis in pharmaceutical products. Analyzing raw materials, intermediates, and finished products using HPLC. Troubleshooting HPLC instrument malfunctions and recommending solutions. Preparing samples for HPLC analysis, including extraction, purification, and quantification. Generating reports and summarizing HPLC data for regulatory submissions , clients or internal use. Operating HPLC Systems: Preparing samples, running analytical experiments, and interpreting results accurately. Method Development and Validation: Developing and validating new HPLC methods for various applications, ensuring compliance with regulatory guidelines. Troubleshooting and Maintenance: Maintaining HPLC instruments, troubleshooting equipment malfunctions, and ensuring optimal performance. Data Analysis: Analyzing HPLC data, generating reports, and interpreting results for further investigation. Collaboration: Working with other scientists and engineers, providing technical support, and contributing to cross-functional projects. Required Skills and Qualifications: Analytical Chemistry: A strong understanding of analytical chemistry principles, including HPLC techniques and chromatography. HPLC Instrumentation: Extensive experience with HPLC instruments, including sample preparation, method development, and maintenance. Problem-Solving: Strong analytical and problem-solving skills to troubleshoot equipment issues and optimize methods. Communication: Effective written and verbal communication skills to document results, report findings, and collaborate with others. Regulatory Knowledge: Familiarity with regulatory guidelines and standards relevant to HPLC and analytical chemistry.
Role Description This is a full-time role for a Quality Control Analyst, based on-site in Pune. The Quality Control Analyst will be responsible for conducting quality control tests, operating laboratory equipment, and ensuring compliance with quality assurance protocols. Day-to-day tasks include analyzing test results, preparing analytical test reports, and maintaining laboratory records. The role requires strict adherence to standard operating procedures to guarantee the accuracy and integrity of data. Skills required - Proficient in Analytical Skills, Quality Control, and Quality Assurance Hands-on experience with Laboratory Skills and Laboratory Equipment Strong attention to detail and problem-solving abilities Excellent communication and documentation skills Bachelor's degree in Chemistry, Biochemistry, or a related field Experience in a GLP-compliant environment is a plus Responsibilities: • Monitor and record daily environment records as per area. • Sample preparation for analysis as per MOA. • Recording of all technical data while preparation of sample such as logbooks, consumption records , worksheets. • Carry out Calculations using Excels • For analyst using instrument needs to maintain cleanliness of instrument. • Loading of sequence on system for GC/HPLC etc. • Required accurate processing of data for HPLC/GC • Required good hands on Excel to carry out all calculations of different tests • Reporting of accurate results of sample with all raw data • Follow GLP and GDP in laboratory • Calibration and maintenance of instrument