Clinical Research Job Vacancies in Nashik

Key ResponsibilitiesQuality Control (QC): Testing raw materials, intermediates, and finished goods to ensure they meet specifications using analytical instruments.Laboratory Testing: Performing chemical assays, titration, pH measurement, viscosity testing, and chromatography (HPLC/GC) as required.Process Monitoring: Tracking chemical reactions on the production floor to ensure temperatures, pressures, and concentrations are maintained.Documentation: Maintaining the Laboratory Notebook and ensuring all test results are recorded accurately in the companys LIMS (Laboratory Information Management System).Compliance & Safety: Handling hazardous chemicals safely, maintaining a clean lab environment, and ensuring compliance with environmental regulations.Calibration: Regularly calibrating lab instruments (balances, spectrophotometers, etc.) to ensure accurate readings.

As a Chemist, you'll be responsible for conducting chemical analyses, experiments, and research in our laboratory. Your primary duties will include performing quality control tests, developing and validating analytical methods, analyzing raw materials and finished products, and documenting findings. This role requires a strong understanding of chemical principles, hands-on experience with laboratory instrumentation, and a meticulous approach to ensure accuracy and compliance.ResponsibilitiesLaboratory Analysis & Testing:Perform routine and non-routine chemical tests and analyses on raw materials, in-process samples, and finished products using various analytical techniques and instrumentation (e.g., HPLC, GC, UV-Vis, Karl Fischer, Titration, pH meter, FTIR specify relevant instruments).Conduct quantitative and qualitative analyses to determine composition, purity, and other chemical properties.Ensure all tests are performed accurately, efficiently, and in accordance with standard operating procedures (SOPs).Quality Control & Assurance:Monitor product quality at various stages of production to ensure compliance with established specifications and quality standards.Identify deviations, out-of-specification results, and non-conformities, and report them promptly.Participate in root cause analysis for quality issues and support corrective and preventive actions (CAPA).Method Development & Validation (if applicable):Develop, optimize, and validate new analytical methods for testing various substances.Verify the accuracy, precision, and robustness of existing analytical methods.Instrumentation Maintenance & Calibration:Perform basic maintenance and calibration of laboratory instruments to ensure their optimal performance and accuracy.Troubleshoot instrument malfunctions and coordinate with service engineers for repairs.Documentation & Reporting:Accurately record all experimental data, observations, and results in lab notebooks and designated systems.Prepare detailed analytical reports, certificates of analysis (CoA), and summaries of findings.Maintain organized laboratory records and documentation for audit purposes.Safety & Compliance:Strictly adhere to all laboratory safety protocols, chemical handling procedures, and waste disposal guidelines.Ensure compliance with Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP if applicable in pharma/food), and other relevant regulatory requirements (e.g., ISO standards).Maintain a clean and organized laboratory workspace.Research & Development Support (if applicable for R&D roles):Assist in research projects, experimental design, and data interpretation for new product development or process improvement.

develop and write trial protocols (outlining purpose and methodology)present trial protocols to a steering committeedesign data collection forms, known as case report forms (CRFs)coordinate with the ethics committee, which safeguards the rights, safety and wellbeing of all trial subjectsmanage regulatory authority applications and approvals that oversee the research and marketing of new and existing drugsidentify and assess the suitability of facilities to use as the clinical trial siteidentify/select an investigator who will be responsible for conducting the trial at the trial siteliaise with doctors, consultants or investigators on conducting the trialset up the trial sites - ensuring each centre has the trial materials, including the trial drug often known as the investigational medicinal product (IMP)train the site staff to trial-specific industry standardsmonitor the trial throughout its duration, which involves visiting the trial sites on a regular basis and dealing with and solving any issuesverify that data entered on to the CRFs is consistent with patient clinical notes, known as source data/document verification (SDV)collect completed CRFs from hospitals and general practiceswrite visit reports and file and collate trial documentation and reportsmeet with team members to discuss on-going trials, results and any trends or adverse eventsensure all unused trial supplies are accounted forclose down trial sites on completion of the trialdiscuss results with a medical statistician, who writes technical trial reportsarchive study documentation and correspondenceprepare final reports and occasionally manuscripts for publication.