72 Job openings found

Key Responsibilities: Conduct routine microbiological testing (water, environment, raw materials, in-process & finished products). Perform environmental monitoring of cleanrooms, utilities, and aseptic areas. Support media fill, sterility testing, endotoxin testing, and microbial limits testing. Ensure compliance with cGMP, SOPs, and regulatory guidelines (USFDA, EU, WHO, etc.). Review and document microbiological data, deviations, and OOS/OOT investigations. Participate ...

Key Responsibilities: Support operation and maintenance of production and utility equipment (e.g., granulators, blenders, tablet compression, coating machines). Assist in monitoring equipment performance and documenting key parameters. Follow Standard Operating Procedures (SOPs) and Good Engineering Practices (GEP). Participate in preventive and breakdown maintenance of machinery and utility systems. Ensure timely documentation of maintenance activities and ...

  Key Responsibilities   1. Sample Analysis and Testing: Perform chemical and instrumental analysis of raw materials, intermediates, and finished API products according to approved specifications and Standard Testing Procedures (STPs). Conduct testing using a range of laboratory instruments, including but not limited to: High-Performance Liquid Chromatography (HPLC) Gas Chromatography (GC) Fourier-Transform Infrared (FT-IR) Spectroscopy Ultraviolet-Visible (UV-Vis) Spectroscopy Karl Fischer ...

To perform all the activities of Quality assurance departments. Ensure that SOPs are available for all quality related activities and they are current. Prepare and review all quality assurance related documents such as SOPs, log book, format, etc. Responsible for the Release of the final products. Review batch sheet, packing sheet and final product ...

Collecting and recording data day to day basis of different trials Compile trial reports Finding vendors for raw material/chemicals Follow up for outside sample testing report/ pending purchase items / vendors for sample/quote Working closely with the development team for planning part Manage testing procedure and validation of new batches Technical content

Responsible for Plant & Utility Instrument Maintenance activity. Responsible for planning to review the SOP, Qualification, Validation, Temperature mapping and other activity. Work permit from respective plants and execute the work as per priority of jobs and type of jobs. Calibration documents review and planning of calibration of instruments. Take trouble shooting action for ...

1. To perform all the activities of Quality assurance departments. 2. Ensure that SOPs are available for all quality related activities and they are current. 3. Prepare and review all quality assurance related documents such as SOPs, log book, format, etc. 4. Responsible for the Release of the final products. 5. Review batch sheet, ...

1. To perform all the activities of Quality assurance departments. 2. Ensure that SOPs are available for all quality related activities and they are current. 3. Prepare and review all quality assurance related documents such as SOPs, log book, format, etc. 4. Responsible for the Release of the final products. 5. Review batch sheet, ...

To follow instructions given by Directors and Factory manager from time to time. Follow formalized SOP and report to Factory Manager and QA in case of any changes or deviation or non-conformity. To coordinate with QC at the time of Calibration. To attend and fix major break down. To coordinate with external agencies for ...

Job description Role & responsibilities   Development of Analytical methods. Validation of Analytical methods. Preparing analytical method development reports. Literature survey for existing analytical methods. Carry out literature survey by establishing the strategies. Maintenance of FDA department. Coordinating various development activities in FDA laboratory. Maintenance of reference standard, working standards and their standardization. Co-ordinating the activities in Chemical and Instrumentation. Analytical Method ...