- Preparation, review and submission of Drug Master Files for various regulated and less regulated markets. - Preparation, review and submission of DMF, Annual updates and submission to US, Canada, China, Korea authorities through online su...
Principal task and Responsibilities: - Process intensification of plant existing batches and upcoming R&D projects. - To find out different strategy of operation to enhance productivity/yield or reduce time cycle and utilization of energy. ...
Major Purpose of the Job: - Routine literature search to understand the reaction condition. - To perform reaction in lab as per Planning given by superior. - LNB writing as per GLP. - To prepare impurity for KSM, intermediate and API as per...
Operate VNA (Very Narrow Aisle) equipment to handle materials in GMP-compliant warehouse racking systems. Perform accurate put-away and retrieval of pharmaceutical materials from designated storage locations. Ensure FIFO/FEFO (First In, Fir...
1. Issue Proforma Invoice for Advance & LC orders & sending PFI to Marketing department for MI. 2. Issue the Bond Invoice to start the process of Packing. 3. Issue the Bar-Codes (GTIN) Label for all Products before shipment is dispatch. 4. ...
Core responsibility related to GLP Study Personnel (Toxicology, in-vivo mutagenicity and Analytical Laboratory) Follow the instructions given in SOPs and study plan and document and communicate any deviation from these instructions directly...
Area Electrophoresis, Immuno Assay and Instrument based test. Role • Responsible for Electrophoresis, Immuno Assay and Instrument based test. • Responsible for Sample Management and related documentation. Job Responsibilities : • Responsibl...
To perform the Technology transfer of Product from R&D to Manufacturing Site. • To perform alternate vendor batch execution, process improvement, change in batch size, trouble shooting at shop floor, equipment change activities of product a...
Core responsibility related to GLP Study Director - Approve the study plan and any amendments to the study plan by dated signature. - Make the study plan available to RQA for verifying that it contains all information required for complianc...
Follow cGMP and GLP practices in Quality Control Lab. • To analyze the Sample of raw material on non-chromatographic instrument such as FTIR, UV, Polarimeter, KF, Autotitrator etc. by following test procedure. • To attend the training as pe...
To set & achieve the daily targets to achieve monthly targets. Trace the daily output of equipment with respect to the daily target and intimate the deviation with justification in OEE report. • To co-ordinate with cross functional departme...