Quality Control Chemist

Role Overview: You will be joining Synnat Pharma Private Limited as a Trainee/Chemist, where your meticulous and detail-oriented approach will be crucial in contributing to the quality control and assurance processes. Your role will involve ensuring that raw materials, in-process materials, and finished products meet stringent quality standards by applying Good Laboratory Practices (GLP) and GMP guidelines. Collaboration with cross-functional teams will be essential in maintaining laboratory standards and compliance requirements, ultimately upholding the integrity of manufacturing processes and delivering high-quality pharmaceutical products. This is an excellent opportunity for you to gain hands-on experience in the pharmaceutical industry and develop a strong foundation in quality control and assurance. Key Responsibilities: - Raw Material Sampling and Analysis - Perform sampling of raw materials following defined procedures to ensure representative collection. - Conduct visual inspections to detect contamination or degradation. - Prepare samples using wet chemistry and instrumental techniques. - Record sampling activities accurately in laboratory notebooks/e-systems. - Compare results to pre-defined specifications and escalate deviations. - Maintain hygiene and safety standards in the sampling area. - In-Process and Finished Product Sampling - Collect in-process material samples during manufacturing according to sampling plans. - Conduct routine testing to monitor key process parameters. - Sample finished API products before QC release. - Document sampling with detailed reports (sample ID, date, process stage). - Collaborate with production and QA to address discrepancies. - Ensure activities align with GMP and regulatory norms. - Laboratory Operations and Compliance - Follow GLP principles to ensure traceability and data integrity. - Maintain detailed records for analyses, calibrations, and maintenance. - Prepare and standardize reagents as per lab SOPs. - Assist during audits and promptly address observations. - Adhere to lab safety protocols and use PPE consistently. - Support method development and validation activities. - Data Analysis and Reporting - Analyze data from techniques like chromatography, spectroscopy, and titrimetry. - Interpret results, identify trends, and flag potential issues. - Prepare summary reports including tables, graphs, and conclusions. - Review and verify analytical data for accuracy. - Share test results with QA, Production, and Regulatory teams. - Maintain secure and accessible databases for analytical data. Qualifications Required: - Possess a Bachelor's or Master's degree in Chemistry, Pharmacy, or a related scientific field. - Foundational understanding of GLP and GMP principles. - Skilled in wet chemistry and basic analytical techniques. - Strong analytical and observational skills to interpret data. - Effective communication and ability to work in team environments. - Proficient in MS Office (Excel, Word, PowerPoint) for reporting. - Highly detail-oriented, quality-focused, and eager to learn.,