Group Lead

3 weeks ago

Hyderabad, India Sai Life Sciences Ltd Full time

- Ensure the good organization and housekeeping of the PRD department work area. - Plan and supervise developmental synthesis of the NCEs / API intermediate / target molecules. - Excel in the observation, recordings and reporting skill sets for the scientific data. - Work as a team and take responsibility with accountability. - Surveys the literature for information concerning specific compounds. - The Feasibility study of custom products involves close monitoring / supervision by research associate. - The Process Optimization shall be made on the selected route based on due diligence and literature during the feasibility studies. - Prior to designing laboratory experiments for process optimization, the MSDS of all input materials shall be obtained and scrutinized for risk assessment. - To improve processes for existing products and improve efficiency in cycle time. - Ensure and sign off the experimental data related to process development studies of the NCEs / API intermediate / target molecules manufacturing are recorded in Electronic Note Book (ELN). - To write process descriptions in the Technical Package and transfer optimized manufacturing strategies to production. - PRD to support the technology transfer team towards the efficient scalability of a given process to the manufacturing site. - To evaluate, recommend new technologies and equipment for synthesis, purification and implement their use in PRD and demonstrate the same to TT. - To support the clients with respect to all the analytical and CMC needs for each project being handled by PRD. - Actively participate in investigation of various complaints and quality related issues like CAPA, closing out the deviations in the manufacturing. - Ensure the good organization and housekeeping of the PRD department work area. - Plan and supervise developmental synthesis of the NCEs / API intermediate / target molecules. - Excel in the observation, recordings and reporting skill sets for the scientific data. - Work as a team and take responsibility with accountability. - Surveys the literature for information concerning specific compounds. - The Feasibility study of custom products involves close monitoring / supervision by research associate. - The Process Optimization shall be made on the selected route based on due diligence and literature during the feasibility studies. - Prior to designing laboratory experiments for process optimization, the MSDS of all input materials shall be obtained and scrutinized for risk assessment. - To improve processes for existing products and improve efficiency in cycle time. - Ensure and sign off the experimental data related to process development studies of the NCEs / API intermediate / target molecules manufacturing are recorded in Electronic Note Book (ELN). - To write process descriptions in the Technical Package and transfer optimized manufacturing strategies to production. - PRD to support the technology transfer team towards the efficient scalability of a given process to the manufacturing site. - To evaluate, recommend new technologies and equipment for synthesis, purification and implement their use in PRD and demonstrate the same to TT. - To support the clients with respect to all the analytical and CMC needs for each project being handled by PRD. - Actively participate in investigation of various complaints and quality related issues like CAPA, closing out the deviations in the manufacturing.

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