Investigation of OOS and OOT results and also involved in handling of deviation. Handling of laboratory incidents and investigation of same. Daily Planning of Work, Maintaining of Laboratory as per GMP. Handling of change control note and CAPA. Handling of Agency & Customer Audit. Planning and managing, day to day analysis of received samples. Ensuring on time release of received samples. Review of Raw material, finished product and Intermediate… Show more Investigation of OOS and OOT results and also involved in handling of deviation. Handling of laboratory incidents and investigation of same. Daily Planning of Work, Maintaining of Laboratory as per GMP. Handling of change control note and CAPA. Handling of Agency & Customer Audit. Planning and managing, day to day analysis of received samples. Ensuring on time release of received samples. Review of Raw material, finished product and Intermediate documents. Review of technology transfer document, specification and STP of products. Review of performance verification, cleaning validation protocol and report. Responsible for Release / Reject the in-process and intermediate products. Responsible to check & sign on the certificate of analysis. Preparation and review of QC documents as per cGMP requirement. Actively involved in instrument calibration activities. Involved in performance qualification of newly installed instruments. Involved in preparation of analytical method validation protocol, test data recording sheet and method validation report. Review of OOS, logically plan hypothesis testing and joint analysis to find out the root cause. Good control on Microsoft office i.e. Excel, Word and power point Show less

Investigation of OOS and OOT results and also involved in handling of deviation.Handling of laboratory incidents and investigation of same.Daily Planning of Work, Maintaining of Laboratory as per GMPHandling of change control note and CAPA. Handling of Agency & Customer AuditPlanning and managing, day to day analysis of received samples. Ensuring on time release of received samples.Review of Raw material, finished product and Intermediate documents.Responsible… Show more Investigation of OOS and OOT results and also involved in handling of deviation.Handling of laboratory incidents and investigation of same.Daily Planning of Work, Maintaining of Laboratory as per GMPHandling of change control note and CAPA. Handling of Agency & Customer AuditPlanning and managing, day to day analysis of received samples. Ensuring on time release of received samples.Review of Raw material, finished product and Intermediate documents.Responsible for Release / Reject the IN process and Intermediate products.Responsible to check & sign on the certificate of analysis.Preparation and review of QC documents as per cGMP requirement.Review of OOS, logically plan hypothesis testing and joint analysis to find out the root cause Good control Microsoft office i.e. Excel, Word and power point Show less

To follow the SOP for stability study of drug product and drug substance.Check the performance of Column and update the list of column.Testing of Stability Samples like tablets and capsules by respective standard testing procedure and by different chromatographic methods like HPLC, Spectrophotometry,etc. and Compilation of Stability Data.To identify area for improving quality of work by training and supporting quality control staff to improve their work performance and suggest cost… Show more To follow the SOP for stability study of drug product and drug substance.Check the performance of Column and update the list of column.Testing of Stability Samples like tablets and capsules by respective standard testing procedure and by different chromatographic methods like HPLC, Spectrophotometry,etc. and Compilation of Stability Data.To identify area for improving quality of work by training and supporting quality control staff to improve their work performance and suggest cost reduction areas and to ensure that the Quality, Health, Safety and Environmental policy and procedures are followed.Conducts a regular inspection on running experiments to check health and safety measures.To follow the GDP, GLP and maintain compliance level in laboratory.Stability sample Documentation and compile the record for the same as per Regulatory requirements and interpret experimental or analytical results.To coordinate OOS, OOT, CCF and deviation related activity.To initiate, investigate and close OOT/OOS and deviation timely. Show less